Reverse-turn mimetics and method relating thereto

ABSTRACT

Conformationally constrained compounds that mimic the secondary structure of reverse-turn regions of biologically active peptides and proteins as well as their prodrugs are disclosed. Such reverse-turn mimetic structures and prodrugs have utility over a wide range of fields, including use as diagnostic and therapeutic agents. Libraries containing the reverse-turn mimetic structures of this invention are also disclosed as well as methods for screening the same to identify biologically active members. The invention also relates to the use of such compounds and prodrugs for inhibiting or treating disorders modulated by Wnt-signaling pathway, such as cancer, especially colorectal cancer, restenosis associated with angioplasty, polycystic kidney disease, aberrant angiogenesis disease, rheumatoid arthritis disease, tuberous sclerosis complex, Alzheimer&#39;s disease, excess hair growth or loss, or ulcerative colitis.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of co-pending U.S. patent application Ser. No. 12/649,161, filed Dec. 29, 2009, which is a continuation of U.S. patent application Ser. No. 11/974,941, filed Oct. 15, 2007 (issued U.S. Pat. No. 7,671,054). The disclosures of these applications are incorporated herein by reference in their entireties.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is 200146_(—)402C11_SEQUENCE_LISTING.txt. The text file is 3 KB, was created on Apr. 7, 2010, and is being submitted electronically via EFS-Web, concurrent with the filing of the specification.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to reverse-turn mimetic structures and to a chemical library relating thereto. The invention also relates to applications in the treatment of medical conditions, e.g., cancer diseases, and pharmaceutical compositions comprising the mimetics.

2. Description of the Related Art

Random screening of molecules for possible activity as therapeutic agents has occurred for many years and resulted in a number of important drug discoveries. While advances in molecular biology and computational chemistry have led to increased interest in what has been termed “rational drug design”, such techniques have not proven as fast or reliable as initially predicted. Thus, in recent years there has been a renewed interest and return to random drug screening. To this end, particular strides having been made in new technologies based on the development of combinatorial chemistry libraries, and the screening of such libraries in search for biologically active members.

In general, combinatorial chemistry libraries are simply a collection of molecules. Such libraries vary by the chemical species within the library, as well as the methods employed to both generate the library members and identify which members interact with biological targets of interest. While this field is still young, methods for generating and screening libraries have already become quite diverse and sophisticated. For example, a recent review of various combinatorial chemical libraries has identified a number of such techniques (Dolle, J. Com. Chem., 2(3): 383-433, 2000), including the use of both tagged and untagged library members (Janda, Proc, Natl. Acad. Sci. USA 91:10779-10785, 1994).

Initially, combinatorial chemistry libraries were generally limited to members of peptide or nucleotide origin. To this end, the techniques of Houghten et al. illustrate an example of what is termed a “dual-defined iterative” method to assemble soluble combinatorial peptide libraries via split synthesis techniques (Nature (London) 354:84-86, 1991; Biotechniques 13:412-421, 1992; Bioorg. Med. Chem. Lett. 3:405-412, 1993). By this technique, soluble peptide libraries containing tens of millions of members have been obtained. Such libraries have been shown to be effective in the identification of opioid peptides, such as methionine- and leucine-enkephalin (Dooley and Houghten, Life Sri. 52, 1509-1517, 1993), and a N-acylated peptide library has been used to identify acetalins, which are potent opioid antagonists (Dooley et al., Proc. Natl. Acad. Sci. USA 90:10811-10815, 1993. More recently, an all D-amino acid opioid peptide library has been constructed and screened for analgesic activity against the mu (“μ”) opioid receptor (Dooley et al, Science 266:2019-2022, 1994).

While combinatorial libraries containing members of peptide and nucleotide origin are of significant value, there is still a need in the art for libraries containing members of different origin. For example, traditional peptide libraries to a large extent merely vary the amino acid sequence to generate library members. While it is well recognized that the secondary structures of peptides are important to biological activity, such peptide libraries do not impart a constrained secondary structure to its library members.

To this end, some researchers have cyclized peptides with disulfide bridges in an attempt to provide a more constrained secondary structure (Tumelty et al., J. Chem. Soc. 1067-68, 1994; Eichler et al., Peptide Res. 7:300-306, 1994). However, such cyclized peptides are generally still quite flexible and are poorly bioavailable, and thus have met with only limited success.

More recently, non-peptide compounds have been developed which more closely mimic the secondary structure of reverse-turns found in biologically active proteins or peptides. For example, U.S. Pat. No. 5,440,013 to Kahn and published PCT Applications Nos. WO94/03494, WO01/00210A1, and WO01/16135A2 to Kahn each disclose conformationally constrained, non-peptidic compounds, which mimic the three-dimensional structure of reverse-turns. In addition, U.S. Pat. No. 5,929,237 and its continuation-in-part U.S. Pat. No. 6,013,458, both to Kahn, disclose conformationally constrained compounds which mimic the secondary structure of reverse-turn regions of biologically active peptides and proteins. The synthesis and identification of conformationally constrained, reverse-turn mimetics and their application to diseases were well reviewed by Obrecht (Advances in Med. Chem., 4, 1-68, 1999).

While significant advances have been made in the synthesis and identification of conformationally constrained, reverse-turn mimetics, there remains a need in the art for small molecules which mimic the secondary structure of peptides. There is also a need in the art for libraries containing such members, as well as techniques for synthesizing and screening the library members against targets of interest, particularly biological targets, to identify bioactive library members.

The present invention also fulfills these needs, and provides further related advantages by providing conformationally constrained compounds which mimic the secondary structure of reverse-turn regions of biologically active peptides and proteins.

Wnt signaling pathway regulates a variety of processes including cell growth, oncogenesis, and development (Moon et al., 1997, Trends Genet, 13, 157-162; Miller et al., 1999, Oncogene 18, 7860-7872; Nusse and Varmus, 1992, Cell 69, 1073-1087; Cadigan and Nusse, 1997, Genes Dev. 11, 3286-3305; Peifer and Polakis, 2000 Science 287, 1606-1609; Polakis 2000, Genes Dev. 14, 1837-1851). Wnt signaling pathway has been intensely studied in a variety of organisms. The activation of TCF4/β-catenin mediated transcription by Wnt signal transduction has been found to play a key role in its biological functions (Molenaar et al., 1996, Cell 86; 391-399; Gat et al., 1998 Cell 95:605-614; Orford et al., 1999 J. Cell. Biol. 146:855-868; Bienz and Clevers, 2000, Cell 103:311-20).

In the absence of Wnt signals, tumor suppressor gene adenomatous polyposis coli (APC) simultaneously interacts with the serine kinase glycogen synthase kinase (GSK)-3β and β-catenin (Su et al., 1993, Science 262, 1734-1737: Yost et al., 1996 Genes Dev. 10, 1443-1454: Hayashi et al., 1997, Proc. Natl. Acad. Sci. USA, 94, 242-247: Sakanaka et al., 1998, Proc. Natl. Acad. Sci. USA, 95, 3020-3023: Sakanaka and William, 1999, J. Biol. Chem. 274, 14090-14093). Phosphorylation of APC by GSK-3β regulates the interaction of APC with β-catenin, which in turn may regulate the signaling function of β-catenin (B. Rubinfeld et al., Science 272, 1023, 1996). Wnt signaling stabilizes β-catenin allowing its translocation to the nucleus where it interacts with members of the lymphoid enhancer factor (LEF1)/T-cell factor (TCF4) family of transcription factors (Behrens et al., 1996 Nature 382, 638-642; Hsu et al., 1998, Mol. Cell. Biol. 18, 4807-4818; Roose et al., 1999 Science 285, 1923-1926).

Recently c-myc, a known oncogene, was shown to be a target gene for β-catenin/TCF4-mediated transcription the et al., 1998 Science 281 1509-1512; Kolligs et al., 1999 MeI. Cell. Biol. 19, 5696-5706). Many other important genes, including cyclin D1, and metalloproteinase, which are also involved in oncogenesis, have been identified to be regulated by TCF4/bata-catenin transcriptional pathway (Crawford et al., 1999, Oncogene 18, 2883-2891; Shtutman et al., 1999, Proc. Natl. Acad. Sci. USA., 11, 5522-5527; Tetsu and McCormick, 1999 Nature, 398, 422-426).

Moreover, overexpression of several downstream mediators of Wnt signaling has been found to regulate apoptosis (Moris et al., 1996, Proc. Natl. Acad. Sci. USA, 93, 7950-7954; He et al., 1999, Cell 99, 335-345: Orford et al. 1999J. Cell. Biol., 146, 855-868; Strovel and Sussman, 1999, Exp. Cell. Res., 253, 637-648). Overexpression of APC in human colorectal cancer cells induced apoptosis (Moris et al., 1996, Proc. Natl. Acad. Sci. USA. 93, 7950-7954), ectopic expression of β-catenin inhibited apoptosis associated with loss of attachment to extracellular matrix (Orford et al, 1999, J. Cell Biol. 146, 855-868). Inhibition of TCF4/β-catenin transcription by expression of dominant-negative mutant of TCF4 blocked Wnt-1-mediated cell survival and rendered cells sensitive to apoptotic stimuli such as anti-cancer agent (Shaoqiong Chen et al., 2001, J. Cell. Biol., 152, 1, 87-96) and APC mutation inhibits apoptosis by allowing constitutive survivin expression, a well-known anti-apoptotic protein (Tao Zhang et al., 2001, Cancer Research, 62, 8664-8667).

Although mutations in the Writ gene have not been found in human cancer, a mutation in APC or β-catenin, as is the case in the majority of colorectal tumors results in inappropriate activation of TCF4, overexpression of c-myc and production of neoplastic growth (Bubinfeld et al, 1997, Science, 275, 1790-1792; Morin et al, 1997, Science, 275, 1787-1790; Casa et al, 1999, Cell. Growth. Differ. 10, 369-376). The tumor suppressor gene (APC) is lost or inactivated in 85% of colorectal cancers and in a variety of other cancers as well (Kinzler and Vogelstein, 1996, Cell 87, 159-170). APC's principal role is that of a negative regulator of the Wnt signal transduction cascade. A center feature of this pathway involves the modulation of the stability and localization of a cytosolic pool of β-catenin by interaction with a large Axin-based complex that includes APC. This interaction results in phosphorylation of β-catenin thereby targeting it for degradation.

CREB binding proteins (CBP)/p300 were identified initially in protein interaction assays, first through its association with the transcription factor CREB (Chrivia et al, 1993, Nature, 365, 855-859) and later through its interaction with the adenoviral-transforming protein E1A (Stein et al, 1990, J. Viol., 64, 4421-4427; Eckner et al, 1994, Genes, Dev., 8, 869-884). CBP had a potential to participate in variety of cellular functions including transcriptional coactivator function (Shikama et al., 1997, Trends. Cell. Biol. 7, 230-236; Janknecht and Hunter, 1996, Nature, 383, 22-23). CBP/p300 potentiates β-catenin-mediated activation of the siamois promoter, a known Wnt target (Hecht et al, 2000, EMBO J. 19, 8, 1839-1850). β-catenin interacts directly with the CREB-binding domain of CBP and β-catenin synergizes with CBP to stimulate the transcriptional activation of TCF4/β-catenin (Ken-Ichi Takemaru and Randall T. Moon, 2000 J. Cell. Biol 149, 2, 249-254).

BRIEF SUMMARY OF THE INVENTION

From this background, it is seen that TCF4/β-catenin and CBP complex of Wnt pathway can be taken as target molecules for the regulation of cell growth, oncogenesis and apoptosis of cells, etc. Accordingly, the present invention addresses a need for compounds that block TCF4/β-catenin transcriptional pathway by inhibiting CBP, and therefore can be used for treatment of cancer, especially colorectal cancer.

In brief, the present invention is directed to a new type of conformationally constrained compounds, which mimic the secondary structure of reverse-turn regions of biologically active peptides and proteins. This invention also discloses libraries containing such compounds, as well as the synthesis and screening thereof.

The compounds of the present invention have the following general formula (I):

wherein A is —(CHR₃)— or —(C═O)—, B is —(CHR₄)— or —(C═O)—, D is —(CHR₅)— or —(C═O)—, E is —(ZR₆)— or —(C═O)—, G is —(XR₇)_(n)—, —(CHR₇)—(NR₈)—, —(C═O)—(XR₉)—, or —(C═O)—, W is —Y(C═O)—, —(C═O)NH—, —(SO₂)— or is absent, Y is oxygen, sulfur, or —NH—, X and Z is independently nitrogen or CH, n=0 or 1; and R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ and R₉ are the same or different and independently selected from an amino acid side chain moiety or derivative thereof, the remainder of the molecule, a linker and a solid support, and stereoisomers thereof.

In an embodiment wherein A is —(CHR₃)— or —(C═O)—; B is —(CHR₄)— or —(C═O)—; D is —(CHR₅)— or —(C═O)—; E is —ZR₆— or —(C═O)—, wherein Z is CH or N; G is —XR₇— or —(C═O)—, wherein X is CH or N; W is —(C═O)NH—, —(C═O)S—, —S(O)₂— or nothing; and each of R₁, R₂, R₃, R₄, R₅, R₆ and R₇ is the same or different and independently an amino acid side chain moiety or an amino acid side chain derivative, the compounds of this invention have the following formula (IA):

Specific examples of R₁, R₂, R₃, R₄, R₅, R₆ and R₇ are provided in the following detailed description.

In an embodiment wherein A is —(CHR₃)—, B is —(C═O)—, D is —(CHR₅)—, E is —(C═O)—, and G is —(XR₇)_(n)—, the compounds of this invention have the following formula (II):

wherein W, X, Y and n are as defined above, and R₁, R₂, R₃, R₅ and R₇ are as defined in the following detailed description.

In an embodiment wherein A is —(C═O)—, B is —(CHR₄)—, D is —(C═O)—, E is —(ZR₆)—, and G is —(C═O)—(XR₉)—, the compounds of this invention have the following formula (III):

wherein W, X and Y are as defined above. Z is nitrogen or CH (with the proviso that when Z is CH, then X is nitrogen), and R₁, R₂, R₄, R₆ and R₉ are as defined in the following detailed description.

In an embodiment wherein A is —(C═O)—, B is —(CHR₄)—, D is —(C═O)—, E is —(ZR₆)—, and G is (XR₇)_(n)—, the compounds of this invention have the following general formula (IV):

wherein W, Y and n are as defined above, Z is nitrogen or CH (when Z is nitrogen, then n is zero, and when Z is CH, then X is nitrogen and n is not zero), and R₁, R₂, R₄, R₆ and R₇, are as defined in the following detailed description.

In an embodiment wherein A is —(C═O)—, B is —(CHR₄)—, D is —(C═O)—, E is —CHR₆—, and G is —XR₇—, wherein X is CH or N, and the compound has a structure of Formula (IVA):

wherein R₁, R₂, R₄, R₆ and R₇ are as defined in the following detailed description.

In an embodiment of compounds of formula (IVA) wherein X is N, the compound has a structure of Formula (IVA₁):

wherein R₁, R₂, R₄, R₆, R₇ are as defined as in the following detailed description.

In certain embodiments, the compounds of this invention have the following general formula (VI):

wherein R_(a), R_(b), and R_(c) are defined in the following detailed description, and X₁, X₂, and X₃ may be the same or different and independently selected from hydrogen, hydroxyl, and halide.

The present invention is also related to prodrugs using the libraries containing one or more compounds of formula (I). A prodrug is typically designed to release the active drug in the body during or after absorption by enzymatic and/or chemical hydrolysis. The prodrug approach is an effective means of improving the oral bioavailability or i.v. administration of poorly water-soluble drugs by chemical derivatization to more water-soluble compounds. The most commonly used prodrug approach for increasing aqueous solubility of drugs containing a hydroxyl group is to produce esters containing an ionizable group; e.g., phosphate group, carboxylate group, alkylamino group (Fleisher et al., Advanced Drug Delivery Reviews, 115-130, 1996; Davis et al., Cancer Res., 7247-7253, 2002, Golik et al., Bioorg. Med. Chem. Lett 1837-1842, 1996).

In certain embodiments, the prodrugs of the present invention have the following general formula (VII): —R₁₀  (VI) wherein (VI) is formula (VI) as described above; one of R_(a), R_(b), R_(c), X₁, X₂, and X₃ is linked to R₁₀ via Y, Y is oxygen, sulfur, or nitrogen in R_(a), R_(b), or R_(c), or an oxygen in X₁, X₂ or X₃; R₁₀ is hydroxyalkyl, glycosyl, phosphoryloxymethyloxycarbonyl, substituted or unsubstituted piperidine carbonyloxy, or a salt thereof; or Y—R₁₀ is an amino acid residue, a combination of amino acid residues, phosphate, hemimalate, hemisuccinate, dimethylaminoalkylcarbamate, dimethylaminoacetate, or a salt thereof; and when not linked to R₁₀, R_(a), R_(b), and R_(c) are as defined in the following detailed description.

In certain embodiments, the prodrugs of the present invention are capable of serving as a substrate for a phosphatase, a carboxylase, or another enzyme and are thereby converted to compounds having general formula (VI).

In some embodiments, R₁₀ of the general formula (VII) is not an amino acid group or a phospho-amino acid group.

The present invention is also directed to libraries containing one or more compounds of formula (I) above, as well as methods for synthesizing such libraries and methods for screening the same to identify biologically active compounds. Compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier or diluent are also disclosed.

The present invention is also related to methods for identifying a biologically active compound using the libraries containing one or more compound of formula (I). In a related aspect, the present invention provides a method for performing a binding assay, comprising (a) providing a composition comprising a first co-activator and an interacting protein, said first co-activator comprising a binding motif of LXXLL, LXXLI or FXXFF wherein X is any amino acid; (b) combining the first co-activator and the interacting protein with a test compound; and (c) detecting alteration in binding between the first co-activator and the interacting protein in the presence of the compound having general formula (I).

The present invention also provides methods for preventing or treating disorders associated with Wnt signaling pathway. Disorders that may be treated or prevented using a compound or composition of the present invention include tumor or cancer (e.g., KSHV-associated tumor), restenosis associated with angioplasty, polycystic kidney disease, aberrant angiogenesis disease, rheumatoid arthritis disease, ulcerative colitis, tuberous sclerosis complex, hair loss, and Alzheimer's disease. Such methods comprise administering to a subject in need thereof a compound or composition of the present invention in an amount effective to achieve the desired outcome.

In a related aspect, the present invention further provides methods for promoting neurite outgrowth, differentiation of a neural stem cell, and apoptosis in cancer cells. Such methods comprise administering to appropriate cells a compound or composition of the present invention in an amount effective to achieve the desired outcome.

These and other aspects of this invention will be apparent upon reference to the attached figure and following detailed description. To this end, various references are set forth herein, which describe in more detail certain procedures, compounds and/or compositions, and are incorporated by reference in their entirety.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 provides a general synthetic scheme for preparing reverse-turn mimetics of the present invention.

FIG. 2 provides a general synthetic scheme for preparing reverse-turn mimetics of the present invention.

FIG. 3 shows a graph based on the measurement of IC₅₀ for Compound A of the present invention using SW480 cells, wherein cell growth inhibition on SW480 cells was measured at various concentrations of Compound A prepared in Example 4 to obtain the IC₅₀ value. Specifically, the degree of inhibition in firefly and renilla luciferase activities by Compound A was determined. As a result, the IC₅₀ of Compound A against SW480 cell growth was found as disclosed in Table 4. Detailed procedures are the same as disclosed in Example 6.

FIG. 4. PC-12 cells were cultured on coated dishes, and differentiated for 10 days in 50 ng/ml nerve growth factor (NGF) (as described in Example 7). (A, B) Vector-transfected PC-12 cells (A) and PC-12 cells overexpressing wt PS-1 (B) exhibit extensive neurite outgrowth after 10 days in NGF. (C) PC-12 cells expressing mutant PS-1/L286V do not display significant neurites under the same culture conditions. (D,E) Immunofluorescence analysis of GAP-43 (as described in Example 7), a molecular marker of neurite outgrowth, demonstrates intense staining for GAP-43 in the neurites (D) of vector-transfected and overexpressing PS-1/WT in PC-12 cells (E). (F) Lack of neurite outgrowth corresponds to weak GAP-43 immunostaining in the mutant cells. Data represent at least two independent experiments. (G) Differentiated cells were transfected with, Topflash, a TCF/β-catenin reporter construct. Cells were lysed, and luciferase activity measured 6 hours post-transfection (as described in Example 7). Data represent the mean of three independent experiments (±SD). Asterisk indicate P<0.05.

FIG. 5. Compound D phenotypically corrects deficient neuronal differentiation in PC-12 overexpressing mutant PS-1/L286V cells. Mutant cells were exposed to 10 μM Compound D, in addition to NGF, during the differentiation period (Misner et al., Proc. Natl. Acad. Sci. USA 98, 11714 (2001)). (A) Neurite elongation and extension are observed in PC-12 cells overexpressing PS-1/L286V upon treatment with Compound D. (B) GAP-43 (green) is significantly elevated in the mutant cells, and is seen in the neurites. (C) Quantitation of neurite outgrowth in PC-12 cells. Number of mutant cells with neurite lengths greater than two cell diameters was less than 10% that of the vector-transfected and overexpressing PS-1/WT in PC-12 cells. Number of mutant PS-1/L286V cells that had the defined neurite lengths was significantly increased, after treatment with 10 μM Compound D. The results are the average (±SD) of three independent determinations. Asterisk indicate P<0.05.

FIG. 6. Ephrin B2 (EphB2) receptor expression. Immunofluorescence analysis and RT-PCR were performed to detect EphB2 receptor expression (as described in Example 7). (A, B) EphB2 receptors are clearly demonstrated in neurites of vector-transfected and overexpressing PS-1/WT cells. The intensity of staining correlates with the high expression level. (C) In contrast, PS-1/L286V PC-12 cells have markedly reduced EphB2 receptor expression. (D) Treatment of mutant cells with Compound D leads to increased EphB2 receptor expression, which is focused at points of neurite outgrowth. (E) Expression of EphB2 receptor has previously been shown to be transcriptionally regulated (Guo et al., J. Neurosci. 17, 4212 (1997).). Lane 1, vector-transfected PC-12 cells, lane 2, overexpressing PS-1/WT cells, lane 3, overexpressing mutant PS-1/L286V cells, lane 4, mutant cells treated with Compound D. RT-PCR analysis indicates message for EphB2 receptor in cells overexpressing mutant PS-1/L286V is decreased compared to those in both the vector-transfected and overexpressing wt PS-1 PC-12 cells. Treatment with 10 μM Compound D upregulates EphB2 message. GAPDH is used an internal control.

FIG. 7. A. Compound D arrests cells in G₁. FACS analysis was performed on SW480 (lower panel) and HCT116 (upper panel) cells treated for 24 hours with either Compound D (25 μM) (right) or control (0.5% DMSO (left). 5.5×10⁶ cells were fixed and stained with propidium iodide (PI). B. Compound D selectively activates caspases in colon carcinoma cell lines. SW480 and HCT116 (left graph) cells (10⁵) along with the normal colonocytes CCD18Co (right graph) were treated with either control (0.5% DMSO) or Compound D (25 μM). 24 hours post treatment, cells were lysed and the caspase-3/7 enzymatic activities were measured. Relative fluorescence units (RFU) were calculated by subtracting the unit values of the blank (control, without cells) from the treated samples (Compound D or control) and plotted.

FIG. 8. Compound D reduces colony growth in soft agar in a dose dependent manner. Increasing concentrations of 5-fluorouracil (5-FU) (0.5-32 μM) and Compound D (0.25-5 μM) were added to SW480 (5000 cells/well) of triplicate wells. Cells were washed and suspended in soft agar growth medium. The number of colonies after 8 days (colonies over 60 μM diameter) were counted and plotted against the compound concentration. Mean±SE of three determinations is indicated. The colony number of control in the absence of the compound was 1,637±71.

FIG. 9. A. Compound C reduces tumor growth in nude mouse model. B. Compound C slightly reduces body weight in nude mouse model.

FIG. 10. The survivin transcriptional activity is upregulated by Wnt1, but knock-down by Compound D. Percent luciferase activities were measured in wildtype, CBP+/−, and p300+/−3T3 cells in the absence of Wnt1 and Compound D, or in the presence of Wnt1, Compound D or both.

FIG. 11. Compound A (right graph) and Compound D (left graph) inhibit the activity of a survivin luciferase reporter in SW480 cells. The luciferase activities under the control of the survivin promoter were measured in SW480 cells treated with compound A or Compound D at various concentrations.

FIG. 12. RT-PCR analysis indicates that Compound D treatment decreases the expression level of the survivin gene.

FIG. 13. Compound D decreases the association of various proteins with the survivin promoter. ChIP assays on SW480 cells treated with either Compound D (25 μM) or control (0.5% DMSO) for 18 hours were performed.

FIG. 14. Compound D decreases survivin expression at the translational level. A. Western blot analysis of extracts of cells treated with vehicle (0.5% DMSO) alone, 10 μM or 25 μM Compound D, or 5 μM 5-FU was performed using survivin 6E4 monoclonal antibody (Cell Signaling Technology). B. Survivin immunofluorescence microscopy. Cultured cancer cells were fixed and stained with anti-survivin green. C. Survivin immunofluorescence microscopy. SW480 cells treated with Compound D were fixed and stained with anti-survivin green.

FIG. 15. Compound D activates the caspase 3 activity (but not the caspase 2 activity) via suppression of the survivin expression. Cultured cells with or without transfection of a construct containing the survivin gene were treated with stausporine (0.5 μM), Compound D (2.5 μM or 5.0 μM), or both. The caspase 2 and caspase 3 activities in these cells were measured.

FIG. 16. Compound D promotes cell death via suppression of the survivin expression. Cultured cancer cells with or without transfection of a construct containing the survivin gene were treated with stausporine (0.5 μM), Compound D (5.0 μM), or both. The cell death of these cells was measured.

FIG. 17. Compound D increases the number of cells in G₀. Cultured cancer cells with or without transfection of a construct containing the survivin gene were treated with stausporine (0.5 μM), Compound D (5 μM), or both. FACS analysis was performed on these cells and the percentages of cells in G₀ are indicated.

FIG. 18 shows the changes of concentrations of prodrug A and its parent compound in mouse plasma with the increase of time after i.v. bolus injection of prodrug A. Square: parent compound; Diamond: prodrug A.

FIG. 19 shows synergy of Compound A and 5-FU in inhibiting tumor cell growth in soft agar assay.

FIG. 20 shows anti-angiogenic activity of Compound E. A: vehicle control; B-F: Compound E at 0.1 μM (B), at 0.3 μM (C), at 1.0 μM (D), at 3 μM (E), and at 10 μM (F); G: Fumagilin at 10 μM.

FIG. 21 shows efficacy of Compound F in rat adjuvant-induced arthritis model.

FIG. 22 shows the effect of Compound F on serum TNF-α concentrations induced by intraperitoneal injection of LPS.

FIG. 23 shows the activity of Compound F in NF-κB reporter assay.

FIG. 24A shows inhibition of LPS-induced TNF-α production in THP-1 cells by Compound F.

FIG. 24B shows inhibition of PMA/Ionomycin induced IL-2 production in Jurkat cells by Compound F.

DETAILED DESCRIPTION OF THE INVENTION

As used in the specification and appended claims, unless specified to the contrary, the following terms have the meaning indicated:

“Amino” refers to the —NH₂ radical.

“Amidino” refers to the —C(═NH)—NH₂ radical. One or both hydrogens of the amine group of the amidino may be replaced with one or two alkyl groups, as defined herein. The alkyl-derivatized amidino radicals are also referred to as “alkylamidino” and “dialkylamidino,” respectively.

“Cyano” refers to the —CN radical,

“Carboxy” refers to the —COOR radical, wherein R is hydrogen or alkyl, as defined herein.

“Acyl” refers to the —COR radical, wherein R is alkyl, aryl, cycloalkyl, heterocyclyl, as defined herein. For example, R can be methyl, butenyl, cyclopropyl, and the like.

“Alkylsulfonate” refers to —S(O)₂—OR radical, wherein R is alkyl, as defined herein.

“Amidosulfonate” refers to the radical —OS(O)₂—NR₂, each R is independently hydrogen or alkyl. Exemplary amidosulfonates include —OS(O)₂NH₂, —OS(O)₂NHMe.

“Aminocarbonyl” refers to the radical —C(O)NR₂, each R is independently hydrogen, alkyl, amino, cycloalkylalkyl, heterocyclyl, alkoxyalkyl, hydroxyalkyl, hydroxy, alkoxy, arylalkyl, heterocyclylalkyl, or two Rs together with the nitrogen atom to which they are attached form a heterocyclyl, as defined herein. When one of the R is hydrogen, the other R is C1-4alkyl, aminocarbonyl can be represented by “C₁₋₄alkylformamidyl”

“N-formamidyl” refers to the radical NHC(O)H.

“Phenylsulfonyl” refers to the —S(O)₂—R radical, wherein R is phenyl, the phenyl can be further substituted with alkyl or chloro.

“Phenylsulfonate” refers to the —O—S(O)₂—R radical, wherein R is phenyl, the phenyl can be further substituted with alkyl or chloro.

“Alkylsulfonyl” refers to the —S(O)₂—R radical, wherein R is alkyl, as defined herein. Exemplary alkylsulfonyl radicals include methylsulfonyl.

“Alkylthio” refers to the —SR radical wherein R is alkyl, as defined herein.

“Arylthio” refers to the SR radical wherein R is aryl, as defined herein. The aryl group of the arylthio can be further substituted with alkyl or chloro.

“Aryloxy” refers to the —OR radical wherein R is aryl, as defined herein. The aryl group can be further substituted with alkyl, alkoxy and the like.

“Acyloxyalkyl” refers to the —R′—OC(O)—R radical, wherein R is alkyl, aryl, cycloalkyl, heterocyclyl, as defined herein; and R′ is an alkylene chain, which is a straight or branched hydrocarbon diradical. Examples of alkylene groups include methylene (—CH₂—), ethylene (—CH₂CH₂—) and the like.

“Guanidino” refers to the —NH—C(═NH)—NH₂ radical. One or both hydrogens of the amine group of the guanidine may be replaced with one or two alkyl groups, as defined herein. The alkyl-derivatized guanidine radicals are also referred to as “alkylguanidino” and “dialkylguanidino,” respectively.

“Nitro” refers to the —NO₂ radical.

“Alkyl” refers to a straight or branched hydrocarbon chain radical consisting solely of carbon and hydrogen atoms. An alkyl may be saturated (containing carbons linked together by single bonds only) or unsaturated (containing carbons linked together by at least one double bond or triple bond.) An alkyl having one to twelve carbon atoms is also referred to as “lower chain alkyl moieties” and can be presented by “C₁₋₁₂alkyl.” In other embodiments, an alkyl may comprise one to four carbon atoms and be represented by “C₁₋₄alkyl.” In other embodiments, an alkyl may comprise two to five carbon atoms and be represented by “C₂₋₅alkyl.” An alkyl is attached to the rest of the molecule by a single bond. Examples of saturated alkyls include, without limitation, methyl, ethyl, n-propyl, 1-methylethyl (iso-propyl), n-butyl, n-pentyl, 1,1-dimethylethyl (t-butyl), 3-methylhexyl, 2-methylhexyl, and the like. Examples of unsaturated alkyls include, without limitation, ethenyl (i.e., vinyl), prop-1-enyl (i.e., allyl), but-1-enyl, pent-1-enyl, penta-1,4-dienyl, ethynyl (i.e., acytylenyl), prop-1-ynyl and the like.

An alkyl may also be a monocyclic or bicyclic hydrocarbon ring radical, which may include fused or bridged ring systems. A cyclic alkyl is also referred to as “cycloalkyl.” In certain embodiments, a cycloalkyl may comprise three to six carbon atoms and be represented by “C₃₋₆cycloalkyl.” Examples of monocyclic cycloalkyl radicals include, e.g., cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl. An unsaturated cycloalkyl contains an endo double bond (i.e., a double bond in the ring). Examples of an unsaturated cycloalkyl include cyclohexenyl. Examples of bicyclic cycloalkyl radicals include, for example, norbornyl (i.e., bicyclo[2.2.1]heptyl), 7,7-dimethyl-bicyclo[2.2.1]heptyl, and the like.

Unless stated otherwise specifically in the specification, the term “alkyl” is meant to include both alkyl and “substituted alkyl,” which refers to an alkyl radical in which one or more hydrogen atoms are replaced by one or more substituents independently selected from: acyl, amidino, alkylamidino, dialkylamidino, alkoxy, aryl, cyano, cycloalkyl, guanidino, alkylguanidino, dialkylguanidino, halo, heterocyclyl, hydrazinyl, hydroxyl, nitro, —OC(O)—R¹¹, —N(R¹¹)₂, —C(O)OR¹¹, —C(O)N(R¹¹)₂, —N(R)C(O)OR¹¹N(R¹¹)C(O)R¹¹, —N(R¹¹)S(O)_(t)R¹¹ (where t is 1 or 2), —S(O)_(t)OR¹¹ (where t is 1 or 2), —S(O)_(p)R¹¹ (where p is 0, 1 or 2), and —S(O)_(t)N(R¹¹)₂ (where t is 1 or 2) where each R¹¹ is independently hydrogen, alkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl, as defined herein.

“Alkoxy” refers to a radical represented by the formula alkyl-C—, wherein alkyl is as defined herein. The alkyl portion can be further substituted by one or more halogen. An alkoxy may also be represented by the number of the carbons in the alkyl group, for example, C₁₋₆alkoxy or C₁₋₃alkoxy.

“Acyl” refers to a radical represented by the formula R¹²C(O)—, wherein R¹² is alkyl or aryl as defined herein. The alkyl or aryl can be optionally substituted with the substituents as described for an alkyl or an aryl group, respectively. Exemplary acyl groups include, without limitation, phenylacyl, benzylacyl, C₁₋₆acyl (e.g., acetyl) and the like.

“Aryl” refers to a radical derived from an aromatic monocyclic or bicyclic ring system by removing a hydrogen atom from a ring carbon atom. The aromatic monocyclic or bicyclic hydrocarbon ring system comprises six to twelve carbon atoms (i.e., C₆₋₁₂ aryl), wherein at least one of the rings in the ring system is fully unsaturated, i.e., it contains a cyclic, delocalized (4n+2) π-electron system in accordance with the Hückel theory. Optionally, one or two ring atoms of the aryl may be heteroatoms selected from nitrogen, oxygen or sulfur. Examples of aryl radicals include, but are not limited to, phenyl and naphthyl. Unless stated otherwise specifically in the specification, the term “aryl” is meant to include both aryl and “substituted aryl,” which refers to an aryl radical in which one or more hydrogen atoms are replaced by one or more substituents independently selected from alkyl, acyl, amidino, amidosulfonate, alkoxy, aryloxy, cyano, guanidines, alkylguanidino, dialkylguanidino, halo, hydrazinyl, hydroxyl, nitro, heterocyclyl, —OC(O)—R¹¹, —N(R¹¹)₂, —C(O)OR¹¹, —C(O)N(R¹¹)₂)C(O)OR¹¹, —N(R¹¹)C(O)R¹¹, —N(R¹¹)S(O)_(t)R¹¹ (where t is 1 or 2), —S(O)_(t)OR¹¹ (where t is 1 or 2), —S(O)_(p)R¹¹ (where p is 0, 1 or 2), and —S(O)_(t)N(R¹¹)₂ (where t is 1 or 2) where each R¹¹ is independently hydrogen, alkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl.

“Arylalkyl” refers to an alkyl radical wherein one or more hydrogens of the alkyl are replaced with one or more aryl groups, as defined herein. In various embodiments, arylalkyls include from 7 to 15 carbons and can be represented by C₇₋₁₅arylalkyl. In certain embodiments, arylalkyl is arylC₁₋₄alkyl wherein a C₁₋₄alkyl is substituted with one aryl or two aryl groups, the latter being also referred to as “diarylalkyl” or “bisarylalkyl”. Examples of arylC₁₋₄alkyl include, but are not limited to arylmethyl, arylethyl, arylpropyl, arylbutyl, bisarylmethyl, bisarylethyl, bisarylpropyl, bisarylbutyl. Exemplary arylalkyl radicals include, without limitation, benzyl, naphthylmethyl, diphenylmethyl, 3,3-bisphenylpropyl and the like. Unless stated otherwise specifically in the specification, the term “arylalkyl” is meant to include both arylalkyl and “substituted arylalkyl,” wherein the alkyl part and/or the aryl part of the arylalkyl radical may be substituted as described herein for the alkyl radical and aryl radical, respectively.

“Cycloalkylalkyl” refers to an alkyl radical wherein one or more hydrogens of the alkyl are replaced with one or more c groups, as defined herein. In certain embodiments, cycloalkylalkyl is cycloalkylC₁₋₂alkyl such as cycloalkylmethyl, cycloalkylethyl and the like. Exemplary cycloalkylalkyl radicals include, without limitation, cyclohexylalkyl (e.g., cyclohexylmethyl and cyclohexylethyl) and cyclopentylalkyl (e.g., cyclopentylmethyl and cyclopentylethyl) and the like. Unless stated otherwise specifically in the specification, the term “cycloalkylalkyl” is meant to include both cycloalkylalkyl and “substituted cycloalkylalkyl,” wherein the alkyl part and/or the cycloalkyl part of the cycloalkylalkyl radical may be substituted as described herein for the alkyl radical and cycloalkyl radical, respectively.

“Glycosyl” refers to a radical by removing the hemiacetal hydroxyl group from a cyclic form of a monosaccharide (e.g., glucose), disaccharide, oligosaccharide (comparing three to ten monosaccharides) or polysaccharide (comprising more than ten monosaccharides.)

“Halo” or “halogen” refers to fluoro, chloro, bromo or iodo radicals.

“Haloalkyl” refers to an alkyl radical, as defined herein, which is substituted by one or more halo radicals, as defined herein. Exemplary haloalkyls include, without limitation: trifluoromethyl, difluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl, 3-bromo-2-fluoropropyl, 1-bromomethyl-2-bromoethyl, and the like. An alkyl substituted with one or more fluoro is also referred to as “perfluoroalkyl,” for example, “perfluoC₁₋₄alkyl.” The alkyl part of the haloalkyl radical may be optionally substituted as defined herein for an alkyl group.

“Heterocyclyl” refers to a stable heterocyclic ring radical that comprises two to eleven carbon atoms and from one to three heteroatoms selected from nitrogen, oxygen and sulfur. In certain embodiments, the heterocyclyl contains one or two heteroatoms. Unless stated otherwise specifically in the specification, the heterocyclyl radical may be a monocyclic or bicyclic ring system, which may include fused or bridged ring systems. In certain embodiments, the heterocyclyl may be a 5-, 6- or 7-membered monocyclic ring. In other embodiments, the heterocyclyl may be an 8-, 9-, 10-, 11- or 12-membered fused bicyclic ring. The heteroatoms in the heterocyclyl radical may be optionally oxidized. One or more nitrogen atoms, if present, may be optionally quaternized. The heterocyclyl radical may be non-aromatic or aromatic (i.e., at least one ring in the heterocyclyl radical has a delocalized (4n+2) π-electron system in accordance with the Hückel theory.) The heterocyclyl may be attached to the rest of the molecule through any atom of the ring(s). Examples of non-aromatic heterocyclyl radicals include, but are not limited to, dioxolanyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl (also referred to as “piperidyl”), piperazinyl, 4-piperidonyl, 3-pyrrolinyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholinyl, and thiamorpholinyl. Examples of aromatic heterocyclyl radicals include, but are not limited to, azepinyl, acridinyl, benzimidazolyl, benzindolyl, 1,3-benzodioxolyl, benzofuranyl, benzooxazolyl, benzoisoxazolyl, benzo[d]thiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, benzo[b][1,4]oxazinyl, 1,4-benzodioxanyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzopyranyl, benzopyrazolyl, benzofuranyl, benzofuranonyl, benzothienyl (benzothiophenyl), benzothieno[3,2-d]pyrimidinyl, benzotriazolyl, carbazolyl, chromone, cinnolinyl, cyclopenta[d]pyrimidinyl, dibenzofuranyl, dibenzothiophenyl, furanyl, furanonyl, furo[3,2-c]pyridinyl, isothiazolyl, imidazolyl, indazolyl, indolyl, indazolyl, isoindolyl, indolinyl, isoindolinyl, isoquinolyl, indolizinyl, isoxazolyl, 5,8-methano-5,6,7,8-tetrahydroquinazolinyl, naphthyridinyl, 1,6-naphthyridinonyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl, oxiranyl, 5,6,6a,7,8,9,10,10a-octahydrobenzo[h]quinazolinyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyl, pyrrolyl, pyrazolyl, pyrazolo[3,4-d]pyrimidinyl, pyridinyl (also referred to as pyridyl), pyrido[3,2-d]pyrimidinyl, pyrido[3,4-d]pyrimidinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, quinazolinyl, quinoxalinyl, quinolinyl, isoquinolinyl, tetrahydroquinolinyl, 1,2,3,4-tetrahydrocarbazolyl, 5,6,7,8-tetrahydroquinazolinyl, thiazolyl, thiadiazolyl, triazolyl, tetrazolyl, triazin-2-yl, thieno[2,3-d]pyrimidinyl, thieno[3,2-d]pyrimidinyl, thieno[2,3-c]pridinyl, and thiophenyl (i.e. thienyl). Unless stated otherwise specifically in the specification, the term “heterocyclyl” is meant to include both heterocyclyl and “substituted heterocyclyl,” which refers to a heterocyclyl radical substituted by one or more substituents selected from alkyl, acyl, oxo (e.g., pyridinonyl, pyrrolidonyl), aryl, arylalkyl, acyloxyalkyl, amidino, alkoxy, cyano, guanidino, alkylguanidino, dialkylguanidino, halo, hydrazinyl, hydroxyl, nitro, —OC(O)—R¹¹, —N(R¹¹)₂, —C(O)OR¹¹, —C(O)N(R¹¹)₂, —N(R¹¹)C(O)OR¹¹, —N(R¹¹)C(O)R¹¹, —N(R¹¹)S(O)_(t)R¹¹ (where t is 1 or 2), —S(O)_(t)OR¹¹ (where t is 1 or 2), —S(O)_(p)R¹¹ (where p is 0, 1 or 2), and —S(O)_(t)N(R¹¹)₂ (where t is 1 or 2) where each R¹¹ is independently hydrogen, alkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl.

“Heterocyclylalkyl” refers to an alkyl radical wherein one or more hydrogens of the alkyl are replaced with one or more heterocyclyl groups, as defined herein. If the heterocyclyl is a nitrogen-containing heterocyclyl, the heterocyclyl may be attached to the alkyl radical at the nitrogen atom. In certain embodiments, the alkyl part of the heterocyclylalkyl contains 1-4 carbon atoms and can be represented by heterocyclylC₁₋₄alkyl. Examples of heterocyclylalkyl radicals include, without limitation, morpholinylalkyl such as morpholinylmethyl, piperidylalkyl such as piperidylmethyl, imidazolidinylalkyl such as imidazolidinylmethyl and the like. Additional examples of heterocyclylalkyl radicals, wherein the heterocyclyl part is aromatic, include, but are not limited to: pyridylmethyl, pyridylethyl, pyndylpropyl, pyridylbutyl, quinolinylmethyl, quinolinylethyl, quinolinyipropyl, quinolinylbutyl, indazolylmethyl, indazolylethyl, indazolylpropyl, indazolylbutyl, benzpyrazolylmethyl, benzpyrazolylethyl, benzpyrazolylpropyl, benzpyrazolylbutyl, isoquinolinylmethyl, isoquinolinylethyl, isoquinolinylpropyl, isoquinolinylbutyl, benzotriazolylmethyl, benzotriazolylethyl, benzotriazolylpropyl, benzotriazolylbutyl and the like. Unless stated otherwise specifically in the specification, the term “heterocyclylalkyl” is meant to include both heterocyclylalkyl and “substituted heterocyclylalkyl,” wherein the alkyl part and/or the heterocyclyl part of the heterocyclylalkyl radical may be substituted as described herein for the alkyl radical and the heterocyclyl radical, respectively.

The compounds, or their pharmaceutically acceptable salts may contain one or more asymmetric centers and may thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)- or, as (D)- or (L)- for amino acids. When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers (e.g., cis or trans.) Likewise, all possible isomers, as well as their racemic and optically pure forms, and all tautomeric forms are also intended to be included.

As used herein, “amino acid” is meant to include naturally occurring α-amino acids and/or unnatural amino acids, such as β-amino acids and homoamino acids. Examples of the amino acids include, but are not limited to: alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, phosphoserine, phosphothreonine, phosphotyrosine, 4-hydroxyproline, hydroxylysine, demosine, isodemosine, gamma-carboxyglutamate, hippuric acid, octahydroindole-2-carboxylic acid, statine, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, penicillamine, ornithine, 3-methylhistidine, norvaline, beta-alanine, gamma-aminobutylic acid, cirtulline, homocysteine, homoserine, methyl-alanine, para-benzoylphenylalanine, phenylglycine, propargyiglycine, sarcosine, methionine sulfone, tert-butylglycine, 3,5-dibromotyrosine and 3,5-diiodotyrosine.

“Amino acid residue” or “amino acid side chain moiety” refers to the portion of an amino acid that remains after losing a water molecule (or alcohol) when the amino acid is condensed with a molecule. Typically, an amino acid is condensed with a molecule, including a compound of any of Formulae (I)-(IV), by forming a peptide bond. In certain embodiments, the amino functional group of the amino acid can be condensed with a carboxylic acid group or its reactive equivalent (e.g., carboxylic anhydride) of the molecule. In other embodiments, the carboxylic acid functional group of the amino acid can be condensed with an amine group of the molecule. Typically, a molecule of water is lost during the formation of the peptide bond. Examples of the “amino acid residues” or “amino acid side chain moiety” include, but are not limited to, residues of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, phosphoserine, phosphothreonine, phosphotyrosine, 4-hydroxyproline, hydroxylysine, demosine, isodemosine, gamma-carboxyglutamate, hippuric acid, octahydroindole-2-carboxylic acid, statine, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, penicillamine, ornithine, 3-methylhistidine, norvaline, beta-alanine, gamma-aminobutylic acid, cirtulline, homocysteine, homoserine, methyl-alanine, para-benzoylphenylalanine, phenylglycine, propargylglycine, sarcosine, methionine sulfone, tert-butylglycine, 3,5-dibromotyrosine, 3,5-diiodotyrosine, glycosylated threonine, glyclosylated serine, and glycosylated asparagine.

An “amino acid side chain derivative” refers to a derivative of any of the amino acid side chain moiety as described in Table 1. In certain embodiments, the amino acid side chain derivative is alkyl, acyl, alkoxy, aryl, arylalkyl, heterocyclyl, or heterocyclylalkyl, as defined herein.

TABLE 1 Amino Acid Side Chain Moiety Amino Acid —H Glycine —CH₃ Alanine —CH(CH₃)₂ Valine —CH₂CH(CH₃)₂ Leucine —CH(CH₃)CH₂CH₃ Isoleucine —(CH₂)₄NH₃ ⁺ Lysine —(CH₂)₃NHC(NH₂)NH₂ ⁺ Arginine

Histidine —CH₂OOO⁻ Aspartic acid —CH₂CH₂COO⁻ Glutamic acid —CH₂CONH₂ Asparagine —CH₂CH₂CONH₂ Glutamine

Phenylalanine

Tyrosine

Tryptophan —CH₂SH Cysteine —CH2CH₂SCH₃ Methionine —CH₂OH Serine —CH(OH)CH₃ Threonine

Proline

Hydroxyproline

A “stereoisomer” refers to a compound made up of the same atoms bonded by the same bonds but having different three-dimensional structures, which are not interchangeable. It is therefore contemplated that various stereoisomers and mixtures thereof and includes “enantiomers,” which refers to two stereoisomers whose molecules are nonsuperimposable mirror images of one another.

A “tautomer” refers to a proton shift from one atom of a molecule to another atom of the same molecule.

“Prodrugs” is meant to indicate a compound that may be converted under physiological conditions or by solvolysis to a biologically active compound described herein. Thus, the term “prodrug” refers to a precursor of a biologically active compound that is pharmaceutically acceptable. A prodrug may be inactive when administered to a subject, but is converted in viva to an active compound, for example, by hydrolysis. The prodrug compound often offers advantages of solubility, tissue compatibility or delayed release in a mammalian organism (see, Bundgard, H., Design of Prodrugs (1985), pp, 7-9, 21-24 (Elsevier, Amsterdam).

A discussion of prodrugs is provided in Higuchi, T., et al., “Pro-drugs as Novel Delivery Systems,” A.C.S. Symposium Series, Vol. 14, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated in full by reference herein.

The term “prodrug” is also meant to include any covalently bonded carriers, which release the active compound in vivo when such prodrug is administered to a mammalian subject. Prodrugs of an active compound, as described herein, may be prepared by modifying functional groups present in the active compound in such a way that the modifications are cleaved, either in routine manipulation or in viva, to the parent active compound. Prodrugs include compounds wherein a hydroxyl, amino or mercapto group is bonded to any group that, when the prodrug of the active compound is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino or free mercapto group, respectively. Examples of the prodrugs include, but are not limited to, acetate, succinate, hemisuccinate, malate, hemimalate, formate and benzoate derivatives of alcohol or amine functional groups in the active compounds and the like. Other examples of the prodrugs include, but are not limited to, amino acid derivatives of alcohol or amine functional groups in the active compounds and the like.

The present invention is directed to conformationally constrained compounds that mimic the secondary structure of reverse-turn regions of biological peptide and proteins (also referred to herein as “reverse-turn mimetics”, and is also directed to chemical libraries relating thereto.

The reverse-turn mimetic structures of the present invention are useful as bioactive agents, including (but not limited to) use as diagnostic, prophylactic and/or therapeutic agents. The reverse-turn mimetic structure libraries of this invention are useful in the identification of bioactive agents having such uses. In the practice of the present invention, the libraries may contain from tens to hundreds to thousands (or greater) of individual reverse-turn structures (also referred to herein as “members”).

In one aspect of the present invention, a reverse-turn mimetic structure disclosed having the following formula (I):

wherein A is —(CHR₃)— or —(C═O)—, B is —(CHR₄)— or —(C═O)—, D is —(CHR₅)— or —(C═O)—, E is —(ZR₆)— or —(C═O)—, G is —(XR₇)_(n)—, —(CHR₇)—(NR₈)—, —(C═O)—(XR₉)—, or —(C═O)—, W is —Y(C═O)—, —(C═O)NH—, —(SO₂)— or nothing, Y is oxygen, sulfur, or —NH—, X and Z is independently nitrogen or CH, n=0 or 1; and R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ and R₉ are the same or different and independently selected from an amino acid side chain moiety or derivative thereof, the remainder of the molecule, a linker and a solid support, and stereoisomers thereof.

In one embodiment, R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ and R₉ are independently selected from the group consisting of aminoC₂₋₅alkyl, guanidineC₂₋₅alkyl, C₁₋₄alkylguanidinoC₂₋₅alkyl, diC₁₋₅alkylguanidino-C₂₋₅alkyl, amidinoC₂₋₅ alkyl, C₁₋₄alkylamidinoC₂₋₅alkyl, diC₁₋₄alkylamidinoC₂₋₅alkyl, C₁₋₃alkoxy, phenyl, substituted phenyl (where the substituents are independently selected from one or more of amino, amidino, guanidine, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), benzyl, substituted benzyl (where the substituents on the benzyl are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), naphthyl, substituted naphthyl (where the substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), bis-phenyl methyl, substituted bis-phenyl methyl (where the substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), pyridyl, substituted pyridyl, (where the substituents are independently selected from one or more of amino amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), pyridylC₁₋₄alkyl, substituted pyridylC₁₋₄alkyl (where the pyridine substituents are independently selected from one or more of amino, amidino, guanidine, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), pyrimidylC₁₋₄alkyl, substituted pyrimidylC₁₋₄alkyl (where the pyrimidine substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), triazin-2-yl-C₁₋₄ alkyl, substituted triazin-2-yl-C₁₋₄alkyl (where the triazine substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), imidazoC₁₋₄alkyl, substituted imidazol C₁₋₄alkyl (where the imidazole substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl or hydroxyl), imidazolinylC₁₋₄alkyl, N-amidinopiperazinyl-N—C₀₋₄alkyl, hydroxyC₂₋₅alkyl, C₁₋₅alkylaminoC₂₋₅alkyl, hydroxyC₂₋₅alkyl, C₁₋₅alkylaminoC₂₋₅alkyl, C₁₋₅dialkylaminoC₂₋₅alkyl, N-amidinopiperidinylC₁₋₄alkyl, 4-aminocyclohexylC₀₋₂alkyl, a bicyclic aryl group having 8 to 11 ring members, which may have 1 to 3 heroatoms selected from nitrogen, oxygen, or sulfur, and saturated or unsaturated C₁₋₆alkyl.

In one embodiment, R₁, R₂, R₆ of E, and R₇, R₈ and R₉ of G are the same or different and represent the remainder of the compound, and R₃ of A, R₄ of B or R₅ of D is selected from an amino acid side chain moiety or derivative thereof. As used herein, the term “remainder of the compound” means any moiety, agent, compound, support, molecule, linker, amino acid, peptide or protein covalently attached to the reverse-turn mimetic structure at R₁, R₂, R₅, R₆, R₇, R₈ and/or R₉ positions. This term also includes amino acid side chain moieties and derivatives thereof.

In another embodiment R₃ of A, R₅ of D, R₆ of E, and R₇, R₈, and R₉ of G are the same or different and represent the remainder of the compound, while one or more of, and in one aspect all of, R₁, R₂ and R₄ of B represent an amino acid sidechain. In this case, the term “remainder of the compound” means any moiety, agent, compound, support, molecule, linker, amino acid, peptide or protein covalently attached to the reverse-turn mimetic structure at R₃, R₅, R₆, R₇, R₆ and/or R₉ positions. This term also includes amino acid side chain moieties and derivatives thereof.

As used herein, the term “remainder of the compound” means any moiety, agent, compound, support, molecule, atom, linker, amino acid, peptide or protein covalently attached to the reverse-turn mimetic structure. This term also includes amino acid side chain moieties and derivatives thereof. In one aspect of the invention, any one or more of the R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ and/or R₉ positions may represent the remainder of the compound. In one aspect of the invention, one or more of R₁, R₂ and R₄ represents an amino acid side chain moiety or a derivative thereof.

In the embodiment where A is —(CHR₃)— or —(C═O)—; B is —(CHR₄)— or —(C═O)—; D is —(CHR₅)— or —(C═O)—; E is —ZR₆— or —(C═O)—, wherein Z is CH or N; G is —XR₇— or —(C═O)—, wherein X is CH or N; W is —(C═O)NH—, —(C═O)O—, —(C═O)S—, —S(O)₂— or nothing; the reverse turn mimetic compound of this invention has a structure of Formula (IA):

Wherein each of R₁, R₇, R₃, R₄, R₅, R₆ and R₇ is the same or different and independently an amino acid side chain moiety or an amino acid side chain derivative. The reverse turn mimetic compound may be present as an isolated stereoisomer or a mixture of stereoisomers or as a pharmaceutically acceptable salt thereof.

In certain embodiments, R₁, R₂, R₃, R₄, R₅, R₆ and R₇ of compounds of formula (IA) are independently: aminoC₂₋₅alkyl, guanidinoC₂₋₅alkyl, C₁₋₄alkylguanidinoC₂₋₅alkyl, diC₁₋₄alkylguanidino-C₂₋₅alkyl, amidinoC₂₋₅alkyl, C₁₋₄alkylamidinoC₂₋₅alkyl, diC₁₋₄alkylamidinoC₂₋₅alkyl, C₁₋₃alkoxy, C₆₋₁₂aryl, C₆₋₁₂arylalkyl, phenyl or substituted phenyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoroC₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; naphthyl or substituted naphthyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoroC₁₋₄alkyl, C₁₋₄alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl; benzyl or substituted benzyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; bisphenylmethyl or substituted bisphenylmethyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; pyridyl or substituted pyridyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; pyridylC₁₋₄alkyl, or substituted pyridylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; pyrimidylC₁₋₄alkyl, or substituted pyrimidylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; triazin-2-ylC₁₋₄alkyl, or substituted triazin-2-ylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; imidazolylC₁₋₄alkyl or substituted imidazolylC₁₋₄alkyl haying one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; or N-amidinopiperazinyl-N—C₀₋₄alkyl, N-amidinopiperidinylC₁₋₄alkyl, or 4-aminocyclohexylC₀₋₂alkyl.

In certain embodiments, R₁, R₂, R₃, R₄, R₅, R₆ and R₇ of compounds of formula (IA) are independently: C₁₋₁₂ alkyl or substituted C₁₋₁₂ alkyl having one or more substituents independently selected from: amino, guanidino, C₁₋₄alkylguanidino, diC₁₋₄alkylguanidino, amidino, C₁₋₄alkylamidino, diC₁₋₄alkylamidino, C₁₋₅alkylamino, diC₁₋₅alkylamino, hydroxy; phenyl or substituted phenyl having one or more substituents independently selected from: amino, guanidino, C₁₋₄alkylguanidino, diC₁₋₄alkylguanidino, amidino, C₁₋₄alkylamidino, diC₁₋₄alkylamidino, C₁₋₅alkylamino, hydroxy; C₁₋₆alkoxy; monocyclic aryl-methyl having 5 to 7 ring members, which may have 1 to 2 heteroatoms selected from nitrogen, oxygen or sulfur, or substituted monocyclic aryl-methyl having one or more substituents independently selected from: halogen, C₁₋₆alkyl, C₁₋₆alkoxy, cyano, hydroxyl; bicyclic aryl-methyl having 8 to 11 ring members, which may have 1 to 2 heteroatoms selected from nitrogen, oxygen or sulfur, or substituted bicyclic aryl-methyl having one or more substituents independently selected from: halogen, C₁₋₆alkyl, C₁₋₆alkoxy, cyano, hydroxyl; or C₁₋₁₂arylalkyl or substituted C₁₋₁₂arylalkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl.

In certain embodiments, R₂ of compounds of formula IA is 3,3-bisphenylpropyl, 2-thienylethyl or tetrahydrofuranylmethyl.

In certain embodiments, R₁, R₂, R₃, R₄, R₅, R₆ and R₇ of compounds of formula (IA) are independently: C₁₋₁₂alkyl or substituted C₁₋₁₂ alkyl having one or more substituents independently selected from acyl, carboxy, alkylthio, and phenylsulfonyl; substituted C₆₋₁₂aryl substituted with amidosulfonate; arylC₁₋₄alkyl or substituted arylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₆cycloalkyl, halogen, perfluoroC₁₋₄alkyl, C₁₋₆alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, C₁₋₆alkyloxyC₁₋₆acyl, morphorlinylC₁₋₆alkyl, aryl, aryloxy, (alkyl)(arylalkyl)amino, heterocyclyl, acyl, amidosulfonate, aminocarbonyl, alkylsulfonate, alkylsulfonyl, alkylthio, arylthio, phenylsulfonate, phenylsulfonyl, morphorlinylC₁₋₃alkoxy, N-formamidyl, and pyrrolidonyl; heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; heterocyclylC₁₋₄alkyl or substituted heterocyclyC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₆cycloalkyl, halogen, perfluoroC₁₋₄alkyl, C₁₋₆alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, C₁₋₆alkyloxyC₁₋₆acyl, morphorlinylC₁₋₆alkyl, arylalkyl, aryl, heterocyclyl, acyl, phenylsulfonyl, cycloalkylalkyl, acyloxyalkyl, aminocarbonyl and C₁₋₄alkylformamidyl; cycloalkyl or substituted cycloalkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; or cycloalkylalkyl or substituted cycloalkylalkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl.

In certain embodiments of the compounds described in the preceding paragraph, arylC₁₋₄alkyl is benzyl, bisphenylmethyl, naphthylmethyl or 3,3-bisphenylpropyl; and heterocyclylC₁₋₄alkyl is benzotriazolylC₁₋₄alkyl, benzopyrazolylC₁₋₄alkyl, indazolylC₁₋₄alkyl, isoquinolylC₁₋₄alkyl, benzothiazolylC₁₋₄alkyl, quinolinylC₁₋₄alkyl, imidazolinylC₁₋₄alkyl, thienylC₁₋₄alkyl, tetrahydrofuranylC₁₋₄alkyl, pyridinylC₁₋₄alkyl, benzimidazolylC₁₋₄alkyl, orindolylC₁₋₄alkyl.

In a further embodiment, and in addition to being an amino acid side chain moiety or derivative thereof (or the remainder of the compound in the case of R₁, R₂, R₃, R₅, R₆, R₇, R₈ and R₉), R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ or R₉ may be a linker facilitating the linkage of the compound to another moiety or compound. For example, the compounds of this invention may be linked to one or more known compounds, such as biotin, for use in diagnostic or screening assay. Furthermore, R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈ or R₉ may be a linker joining the compound to a solid support (such as a support used in solid phase peptide synthesis) or alternatively, may be the support itself. In this embodiment, linkage to another moiety or compound, or to a solid support, is preferable at the R₁, R₂, R₇ or R₈, or R₉ position, and more preferably at the R₁ or R₂ position.

In the embodiment wherein A is —(CHR₃)—, B is —(C═O)—, D is —(CHR₅)—, E is —(C═O)—, and G is —(XR₇)_(n)—, the reverse turn mimetic compound of this invention has the following formula (II):

wherein R₁, R₂, R₃, R₅, R₇, W, X and n are as defined above. In a preferred embodiment, R₁, R₂ and R₇ represent the remainder of the compound, and R₃ or R₅ is selected from an amino acid side chain moiety.

In the embodiment wherein A is —(C═O)—, B is —(CHR₄)—, is —(C═O)—, E is —(ZR₆)—, G is —(C═O)—(XR₉)—, the reverse turn mimetic compound of this invention has the following general formula (III):

wherein R₁, R₂, R₄, R₆, R₉, W and X are as defined above, Z is nitrogen or CH (when Z is CH, then X is nitrogen). In a preferred embodiment, R₁, R₂, R₆ and R₉ represent the remainder of the compound, and R₄ is selected from an amino acid side chain moiety.

In a more specific embodiment wherein A is —(C═O)—, B is —(CHR₄)— D is —(C═O)—, E is —(ZR₆)—, and G is (XR₇)_(n)—, the reverse turn mimetic compound of this invention has the following formula (IV):

wherein R₁, R₂, R₄, R₆, R₇, W, X and n are as defined above, and Z is nitrogen or CH. In certain embodiments, when Z is nitrogen, then n is zero; and when Z is CH, then X is nitrogen and n is not zero. In a preferred embodiment, R₁, R₂, R₆ and R₇ represent the remainder of the compound, and R₄ is selected from an amino acid side chain moiety. In one aspect, R₆ or R₇ is selected from an amino acid side chain moiety when Z and X are both CH.

In the embodiment wherein A is —(C═O)—, B is —(CHR₄)—, D is —(C═O)—, E is —CHR₆—, G is —XR₇—, and X is CH or N, the compound has a structure of Formula (IVA):

wherein each of R₁, R₂, R₄, R₆ and R₇ is the same or different and independently an amino acid side chain moiety or an amino acid side chain derivative.

In the embodiment wherein A is —(C═O)—, B is —(CHR₄)—, D is —(C═O)—, E is —CHR₆—, G is —XR₇—, and X is N the compound has a structure of Formula (IVA₁):

wherein each of R₁, R₂, R₄, R₆ and R₇ is the same or different and independently an amino acid side chain moiety or an amino acid side chain derivative.

In certain embodiments of the compounds of formula (IVA₁), R₁, R₂, R₄, R₆, R₇ are independently: C₁₋₁₂alkyl or substituted C₁₋₁₂ alkyl having one or more substituents independently selected from: amino, guanidino, C₁₋₄alkylguanidino, diC₁₋₄alkylguanidino, amidino, C₁₋₄alkylamidino, diC₁₋₄alkylamino, C₁₋₅alkylamino, diC₁₋₅alkylamino and hydroxy; phenyl or substituted phenyl having one or more substituents independently selected from: amino, guanidino, C₁₋₄alkylguanidino, diC₁₋₄alkylguanidino, amidino, C₁₋₄alkylamidino, diC₁₋₄alkylamidino, C₁₋₅alkylamino, diC₁₋₅alkylamino, hydroxy; C₁₋₆alkoxy; monocyclic aryl-methyl having 5 to 7 ring members, which may have 1 to 2 heteroatoms selected from nitrogen, oxygen or sulfur, or substituted monocyclic aryl-methyl having one or more substituents independently selected from: halogen, C₁₋₆alkyl, C₁₋₆alkoxy, cyano and hydroxyl; bicyclic aryl-methyl having 8 to 11 ring members, which may have 1 to 2 heteroatoms selected from nitrogen, oxygen or sulfur, or substituted bicyclic aryl-methyl having one or more substituents independently selected from: halogen, C₁₋₆alkyl, C₁₋₆alkoxy, cyano, hydroxyl; or C₁₋₁₂arylalkyl or substituted C₁₋₁₂arylalkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl.

In certain embodiments of the compounds of formula (IVA₁), each of R₁ and R₄ is independently alkyl, aryl, arylalkyl, heterocyclylalkyl or phenol-methyl; R₂ is substituted C₁₋₁₂alkyl having one or more substituents independently selected from: C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoroC₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, acyl and phenylsulfonyl; arylC₁₋₄alkyl or substituted arylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, aryl, aryloxy, (alkyl)(arylalkyl)amino, heterocyclyl, acyl, amidosulfonate, aminocarbonyl, alkylsulfonate, alkylsulfonyl, alkylthio, arylthia, phenylsulfonate, phenylsulfonyl, morphorlinylC₁₋₃alkoxy, N-formamidyl and pyrrolidonyl; heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl and hydroxyl; or heterocyclylC₁₋₄alkyl or substituted heterocyclylC₁₋₄alkyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, arylalkyl, aryl, heterocyclyl, acyl, phenylsulfonyl, cycloalkylalkyl, acyloxyalkyl, aminocarbonyl and C1-4-alkylformamidyl; R₆ is hydrogen or alkyl; and R₇ is hydrogen, alkyl or arylalkyl.

These compounds may be prepared by utilizing appropriate starting component molecules (hereinafter referred to as “component pieces”). Briefly, in the synthesis of reverse-turn mimetic structures having formula (I), first and second component pieces are coupled to form a combined first-second intermediate, if necessary, third and/or fourth component pieces are coupled to form a combined third-fourth intermediate (or, if commercially available, a single third intermediate may be used), the combined first-second intermediate and third-fourth intermediate (or third intermediate) are then coupled to provide a first-second-third-fourth intermediate (or first-second-third intermediate) which is cyclized to yield the reverse-turn mimetic structures of this invention. Alternatively, the reverse-turn mimetic structures of formula (I) may be prepared by sequential coupling of the individual component pieces either stepwise in solution or by solid phase synthesis as commonly practiced in solid phase peptide synthesis.

Specific component pieces and the assembly thereof to prepare compounds of the present invention are illustrated in FIG. 1. For example, a “first component piece” may have the following formula S1:

wherein R₂ is as defined above, and R is a protective group suitable for use in peptide synthesis, where this protection group may be joined to a polymeric support to enable solid-phase synthesis. Suitable R groups include alkyl groups and, in a preferred embodiment, R is a methyl group. In FIG. 1, one of the R groups is a polymeric (solid) support, indicated by “Pol” in the Figure. Such first component pieces may be readily synthesized by reductive amination of H₂N—R₂ with CH(OR)₂—CHO, or by a displacement reaction between H₂N—R₂ and CH(OR)₂—CH₂-LG (wherein LG refers to a leaving group, e.g., a halogen (Hal) group).

A “second component piece” may have the following formula S2:

where P is an amino protection group suitable for use in peptide synthesis, L₃ is hydroxyl or a carboxyl-activation group, and R₄ is as defined above. Preferred protection groups include t-butyl dimethylsilyl (TBDMS), t-butyloxycarbonyl (BOC), methyloxycarbonyl (MOC), 9H-fluorenylmethyloxycarbonyl (FMOC), and allyloxycarbonyl (Alloc). N-Protected amino acids are commercially available; for example, FMOC amino acids are available from a variety of sources. In order for the second component piece to be reactive with the first component piece, L₁ is a carboxyl-activation group, and the conversion of carboxyl groups to activated carboxyl groups may be readily achieved by methods known in the art for the activation of carboxyl groups. Suitable activated carboxylic acid groups include acid halides where L₁ is a halide such as chloride or bromide, acid anhydrides where L₁ is an acyl group such as acetyl, reactive esters such as an N-hydroxysuccinimide esters and pentafluorophenyl esters, and other activated intermediates such as the active intermediate formed in a coupling reaction using a carbodiimide such as dicyclohexylcarbodiimide (DCC). Accordingly, commercially available N-protected amino acids may be converted to carboxylic activated forms by means known to one of skill in the art.

In the case of the azido derivative of an amino acid serving as the second component piece, such compounds may be prepared from the corresponding amino acid by the reaction disclosed by Zaloom et al. (J. Org, Chem. 46:5173-76, 1981).

Alternatively, the first component piece of the invention may have the following formula S1′:

wherein R is as defined above and L₂ is a leaving group such as halogen atom or tosyl group, and the second component piece of the invention may have the following formula S2′:

wherein R₂, R₄ and P are as defined above.

A “third component piece” of this invention may have the following formula S3:

where G, E, L₁ and L₂ are as defined above. Suitable third component pieces are commercially available from a variety of sources or can be prepared by methods well known in organic chemistry.

In FIG. 1, the compound of formula (I) has —(C═O)— for A, —(CHR₄)— for B, —(C═O)— for D, and —(CR₆)— for E. Compounds of formula (I) wherein a carbonyl group is at position B and an R group is at position B, i.e., compounds wherein A is —(CHR₃)— and B is —(C═O)—, may be prepared in a manner analogous to that shown in FIG. 1, as illustrated in FIG. 2. FIG. 2 also illustrates adding a fourth component piece to the first-second-third component intermediate, rather than attaching the fourth component piece to the third component piece prior to reaction with the first-second intermediate piece. In addition, FIG. 2 illustrates the preparation of compounds of the present invention wherein D is —(CHR₅)— (rather than (C═O)— as in FIG. 1), and E is —(C═O)— (rather than —(CHR₆)— as in FIG. 1). Finally, FIG. 2 illustrates the preparation of compounds wherein G is NR₇.

Thus, as illustrated above, the reverse-turn mimetic compounds of formula (I) may be synthesized by reacting a first component piece with a second component piece to yield a combined first-second intermediate, followed by reacting the combined first-second intermediate with third component pieces sequentially to provide a combined first-second-third-fourth intermediate, and then cyclizing this intermediate to yield the reverse-turn mimetic structure.

The syntheses of representative component pieces of this invention are described in Preparation Examples and working Examples.

The reverse-turn mimetic structures of formula (III) and (IV) may be made by techniques analogous to the modular component synthesis disclosed above, but with appropriate modifications to the component pieces.

The reverse-turn mimetic structures of the present invention are useful as bioactive agents, such as diagnostic, prophylactic, and therapeutic agents. For example, the reverse-turn mimetic structures of the present invention may be used for modulating a cell signaling transcription factor related peptides in a warm-blooded animal, by a method comprising administering to the animal an effective amount of the compound of formula (I).

Further, the reverse-turn mimetic structures of the present invention may also be effective for inhibiting peptide binding to PTB domains in a warm-blooded animal; for modulating G protein coupled receptor (GPCR) and ion channel in a warm-blooded animal; for modulating cytokines in a warm-blooded animal.

It has been found that the compounds of the formula (I), especially compounds of formula (VI) are effective for inhibiting or treating disorders modulated by Wnt-signaling pathway, such as cancer, especially colorectal cancer.

Formula (VI) is shown above, wherein each of R_(a), R_(b), and R_(c) is the same or different and independently an amino acid side chain moiety or an anima acid side chain derivative, and X₁, X₂, and X₃ may be the same or different and independently selected from hydrogen, hydroxyl, and halide.

In certain embodiments of the compounds of formula (VI), R_(a) is a phenyl group; a substituted phenyl group having one or more substituents wherein the one or more substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl groups; a benzyl group; a substituted benzyl group with one or more substituents where the one or more substituents are independently selected from one or more of amino, amidino, guanidino, hydrazino, amidazonyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl group; or a bicyclic aryl group having 8 to 11 ring members, which may have 1 to 3 heteroatoms selected from nitrogen, oxygen or sulfur; R_(b) is a monocyclic aryl group having 5 to 7 ring members, which may have 1 to 2 heteroatoms selected from nitrogen, oxygen or sulfur, and aryl ring in the compound may have one or more substituents selected from a group consisting of halide, hydroxy, cyano, lower alkyl, and lower alkoxy groups; Rc is a saturated or unsaturated C₁₋₆alkyl, C₁₋₆alkoxy, perfluoro C₁₋₆alkyl, group; and X₁, X₂, and X₃ may be the same or different and independently selected from hydrogen, hydroxyl, and halide.

In certain other embodiments of the compounds of formula (VI), R_(a) is C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoroC₁₋₄alkyl, C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, phenyl substituted with C₃₋₆cycloalkyl, aryl, aryloxy, (alkyl)(arylalkyl)amino, heterocyclyl, acyl, amidosulfonate, aminocarbonyl, alkylsulfonate, alkylsulfonyl, alkylthio, arylthio, phenylsulfonate, phenylsulfonyl, morphorlinylC₁₋₃alkoxy or N-formamidyl; naphthyl or substituted naphthyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₅cycloalkyl, halogen, perfluoroC₁₋₄alkyl, C₁₋₆alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, C₁₋₆alkyloxyC₁₋₆acyl and morphorlinylC₁₋₆alkyl; heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: C₁₋₆alkyl, C₃₋₆cycloalkyl, C₁₋₆alkyloxyC₁₋₆acyl, morphorlinylC₁₋₆alkyl, amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₆cycloalkyl, halogen, nitro, arylalkyl, aryl, heterocyclyl, acyl, phenylsulfonyl, cycloalkylalkyl, acyloxyalkyl, aminocarbonyl and C₁₋₄alkylformamidyl; C₁₋₆acyl; phenylacyl or substituted phenylacyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₃₋₆cycloalkyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl; benzylacyl or substituted benzylacyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, and cyclopropyl; or phenylsulfonyl or substituted phenylsulfonyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₃₋₆cycloalkyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl; R_(b) is aryl or substituted aryl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy; or heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy; R_(c) is C₁₋₆alkyl, C₁₋₆alkoxy, or perfluoroC₁₋₆alkyl; and each of X₁, X₂ and X₃ is independently hydrogen, hydroxyl or halogen.

In certain embodiments of the compounds of formula (VI), especially the compounds described in the preceding paragraph, R_(a) is heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, C₁₋₄alkylformamidyl and C₁₋₆alkoxy, wherein heterocyclyl is pyridyl, quinolinyl, indazolyl, benzpyrazolyl, indolyl, or isoquinolinyl; and R_(b) is pyridyl or substituted pyridyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl and C₁₋₆alkoxy; or piperidyl or substituted piperidyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy.

In another aspect, the present invention provides a pharmaceutical composition comprising a safe and effective amount of the compound having general formula (I) (e.g., the compounds having general formula (IA), (II), (III), (IV), (IVA), (IVA1), and (VI) described above, and the compounds having formula (IVa) and (VII) as described below) and a pharmaceutically acceptable carrier. Such a pharmaceutical composition can be used for treatment of disorders modulated by Wnt signaling pathway, especially by TCF4-β-catenin-CBP complex.

Further, the present invention is to provide a method for inhibiting the growth of tumor cells by using the compound or composition described herein; a method for inducing apoptosis of tumor cells by using the compound or composition described herein; a method for treating a disorder modulated by TCF4-β catenin-CBP complex by using the compound or composition described herein; and a method of treating cancer such as colorectal cancer by administering the compound or composition described herein together with other anti-cancer agent such as 5-fluorouracil (5-FU), taxol, cisplatin, mitomycin C, tegafur, raltitrexed, capecitabine, and irinotecan, etc.

In a preferred embodiment of the present invention, the compound of the present invention has a (6S,10R)-configuration as follows:

wherein R_(a) and R_(b) have the same meanings as defined above.

In another aspect of this invention, prodrugs derived from compounds having general formula (I) are disclosed. The prodrugs generally increase aqueous solubility and thus bioavailability of compounds having general formula (I). In certain embodiments, the prodrugs of the present invention have the following general formula (VII): (VI)-R₁₀  (VII)

wherein one of R_(a), R_(b), R_(c), X₁, X₂, and X₃ is linked to R₁₀ via Y, wherein Y is an oxygen, sulfur, or nitrogen in R_(a), R_(b), or R_(c), or an oxygen in X₁, X₂, or X₃, and R₁₀ is hydroxyalkyl, glycosyl, phosphoryloxymethyloxycarbonyl, substituted or unsubstituted piperidine carbonyloxy, or a salt thereof; or Y—R₁₀ is an amino acid residue, a combination of amino acid residues, phosphate, hemimalate, hemisuccinate, dimethylaminoalkylcarbamate, dimethylaminoacetate, or a salt thereof; and when not linked to R₁₀, R_(a), R_(b), and R_(c) are defined as they are in formula (VI).

For example, in certain embodiments of the compounds of formula (VII), R_(a) is C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoroC₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, phenyl substituted with C₃₋₆cycloalkyl or alkylthio; naphthyl or substituted naphthyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₆cycloalkyl, halogen, perfluoroC₁₋₄alkyl, C₁₋₆alkoxy, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, hydroxyl, C₁₋₆alkyloxyC₁₋₆acyl and morphorlinylC₁₋₆alkyl; heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: C₁₋₆alkyl, C₃₋₆cycloalkyl, C₁₋₆alkyloxyC₁₋₆acyl, morphorlinylC₁₋₆alkyl, amino, amidino, guanidino, hydrazino, C₁₋₄alkylamino, C₁₋₄dialkylamino, C₃₋₆cycloalkylalkyl, halogen, nitro, acyl, phenylsulfonyl, morpholinylC₁₋₃alkoxy, aryl, arylalkyl, and C₁₋₄alkylformamidyl; C₁₋₆acyl; phenylacyl or substituted phenylacyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₃₋₆cycloalkyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl; benzylacyl or substituted benzylacyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, and cyclopropyl; or phenylsulfonyl or substituted phenylsulfonyl having one or more substituents independently selected from: amino, amidino, guanidino, hydrazino, C₃₋₆cycloalkyl, C₁₋₄alkylamino, C₁₋₄dialkylamino, halogen, perfluoro C₁₋₄alkyl, C₁₋₃alkoxy, nitro, carboxy, cyano, sulfuryl, and hydroxyl; R_(b) is aryl or substituted aryl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy; or heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy; R_(c) is C₁₋₆alkyl, C₁₋₆alkoxy, or perfluoroC₁₋₆alkyl; and each of X₁, X₂ and X₃ is independently hydrogen, hydroxyl or halogen.

In certain embodiments of the compounds of formula (VII), especially, the compounds described in the preceding paragraph, R_(a) is heterocyclyl or substituted heterocyclyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, C₁₋₄alkylformamidyl and C₁₋₆alkoxy, wherein heterocyclyl is pyridyl, quinolinyl, indazolyl, benzopyrazolyl, indolyl, or isoquinolinyl; and R_(b) is pyridyl or substituted pyridyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl and C₁₋₆alkoxy; or piperidyl or substituted piperidyl having one or more substituents independently selected from: halogen, hydroxy, cyano, C₁₋₆alkyl, and C₁₋₆alkoxy.

In another aspect of this invention, libraries containing reverse-turn mimetic structures of the present invention are disclosed. Once assembled, the libraries of the present invention may be screened to identify individual members having bioactivity. Such screening of the libraries for bioactive members may involve; for example, evaluating the binding activity of the members of the library or evaluating the effect the library members have on a functional assay. Screening is normally accomplished by contacting the library members (or a subset of library members) with a target of interest, such as, for example, an antibody, enzyme, receptor or cell line. Library members which are capable of interacting with the target of interest, are referred to herein as “bioactive library members” or “bioactive mimetics”. For example, a bioactive mimetic may be a library member which is capable of binding to an antibody or receptor, or which is capable of inhibiting an enzyme, or which is capable of eliciting or antagonizing a functional response associated, for example, with a cell line. In other words, the screening of the libraries of the present invention determines which library members are capable of interacting with one or more biological targets of interest. Furthermore, when interaction does occur, the bioactive mimetic (or mimetics) may then be identified from the library members. The identification of a single (or limited number) of bioactive mimetic(s) from the library yields reverse-turn mimetic structures which are themselves biologically active, and thus are useful as diagnostic, prophylactic or therapeutic agents, and may further be used to significantly advance identification of lead compounds in these fields.

Synthesis of the peptide mimetics of the library of the present invention may be accomplished using known peptide synthesis techniques, in combination with the first, second and third component pieces of this invention. More specifically, any amino acid sequence may be added to the N-terminal and/or C-terminal of the conformationally constrained reverse-turn mimetic. To this end, the mimetics may be synthesized on a solid support (such as PAM resin) by known techniques (see, e.g., John M. Stewart and Janis D. Young, Solid Phase Peptide Synthesis, 1984, Pierce Chemical Comp., Rockford, Ill.) or on a silyl-linked resin by alcohol attachment (see Randolph et al J. Am. Chem. Soc. 117:5712-14, 1995).

In addition, a combination of both solution and solid phase synthesis techniques may be utilized to synthesize the peptide mimetics of this invention. For example, a solid support may be utilized to synthesize the linear peptide sequence up to the point that the conformationally constrained reverse-turn is added to the sequence. A suitable conformationally constrained reverse-turn mimetic structure which has been previously synthesized by solution synthesis techniques may then be added as the next “amino acid” to the solid phase synthesis (i.e., the conformationally constrained reverse-turn mimetic, which has both an N-terminus and a C-terminus, may be utilized as the next amino acid to be added to the linear peptide). Upon incorporation of the conformationally constrained reverse-turn mimetic structures into the sequence, additional amino acids may then be added to complete the peptide bound to the solid support. Alternatively, the linear N-terminus and C-terminus protected peptide sequences may be synthesized on a solid support, removed from the support, and then coupled to the conformationally constrained reverse-turn mimetic structures in solution using known solution coupling techniques.

In another aspect of this invention, methods for constructing the libraries are disclosed. Traditional combinatorial chemistry techniques (see, e.g., Gallop et al., J. Med. Chem. 37:1233-1251, 1994) permit a vast number of compounds to be rapidly prepared by the sequential combination of reagents to a basic molecular scaffold. Combinatorial techniques have been used to construct peptide libraries derived from the naturally occurring amino acids. For example, by taking 20 mixtures of 20 suitably protected and different amino acids and coupling each with one of the 20 amino acids, a library of 400 (i.e., 20²) dipeptides is created. Repeating the procedure seven times results in the preparation of a peptide library comprised of about 26 billion (i.e., 20⁸) octapeptides.

Specifically, synthesis of the peptide mimetics of the library of the present invention may be accomplished using known peptide synthesis techniques, for example, the General Scheme of [4,4,0] Reverse-Turn Mimetic Library as follows:

Synthesis of the peptide mimetics of the libraries of the present invention was accomplished using a FlexChem Reactor Block which has 96 well plates by known techniques. In the above scheme ‘Pol’ represents a bromoacetal resin (Advanced ChemTech) and detailed procedure is illustrated below.

Step 1

A bromoacetal resin (37 mg, 0.98 mmol/g) and a solution of R₂-amine in DMSO (1.4 mL) were placed in a Robbins block (FlexChem) having 96 well plates. The reaction mixture was shaken at 60° C. using a rotating oven [Robbins Scientific] for 12 hours. The resin was washed with DMF, MeOH, and then. DCM

Step 2

A solution of commercial available FmocAmino Acids (4 equiv.), PyBob (4 equiv.), HOAt (4 equiv.), and DIEA (12 equiv.) in DMF was added to the resin. After the reaction mixture was shaken for 12 hours at room temperature, the resin was washed with DMF, MeOH, and then DCM.

Step 3

To the resin swollen by DMF before reaction was added 25% piperidine in DMF and the reaction mixture was shaken for 30 min at room temperature. This deprotection step was repeated again and the resin was washed with DMF, Methanol, and then DCM. A solution of hydrazine acid (4 equiv.), HOBt (4 equiv.), and DIC (4 equiv.) in DMF was added to the resin and the reaction mixture was shaken for 12 hours at room temperature. The resin was washed with DMF, MeOH, and then DCM.

Step 4a (Where Hydrazine Acid is MOC Carbamate)

The resin obtained in Step 3 was treated with formic acid (1.2 mL each well) for 18 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under a reduced pressure using SpeedVac [SAVANT] to give the product as oil. The product was diluted with 50% water/acetonitrile and then lyophilized after freezing.

Step 4b (Where Fmoc Hydrazine Acid is Used to Make Urea Through Isocynate)

To the resin swollen by DMF before reaction was added 25% piperidine in DMF and the reaction mixture was shaken for 30 min at room temperature. This deprotection step was repeated again and the resin was washed with DMF, Methanol, then DCM. To the resin swollen by DCM before reaction was added isocynate (5 equiv.) in DCM. After the reaction mixture was shaken for 12 hours at room temperature the resin was washed with DMF, MeOH, then DCM. The resin was treated with formic acid (1.2 mL each well) for 18 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under a reduced pressure using SpeedVac [SAVANT] to give the product as oil. The product was diluted with 50% water/acetonitrile and then lyophilized after freezing.

Step 4c (Where Fmoc-Hydrazine Acid is Used to Make Urea Through Active Carbamate)

To the resin swollen by DMF before reaction was added 25% piperidine in DMF and the reaction mixture was shaken for 30 min at room temperature. This deprotection step was repeated again and the resin was washed with DMF, MeOH, and then DCM. To the resin swollen by DCM before reaction was added p-nitrophenyl chloroformate (5 equiv.) and diisopropyl ethylamine (5 equiv.) in DCM. After the reaction mixture was shaken for 12 hours at room temperature, the resin was washed with DMF, MeOH, and then DCM. To the resin was added primary amines in DCM for 12 hours at room temperature and the resin was washed with DMF, MeOH, and then DCM. After reaction the resin was treated with formic acid (1.2 mL each well) for 18 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under a reduced pressure using SpeedVac [SAVANT] to give the product as oil. The product was diluted with 50% water/acetonitrile and then lyophilized after freezing.

To generate these block libraries the key intermediate hydrazine acids were synthesized according to the procedure illustrated in Preparation Examples.

Tables 2A, 2B and 2C show a [4,4,0] Reverse turn mimetics library which can be prepared according to the present invention, of which representative preparation is given in Example 4.

TABLE 2A THE [4,4,0] REVERSE TURN MIMETICS LIBRARY

Mol. No R₂ R₄ R₇ R₁—Y′ Weight M + H 1 2,4-Cl₂-benzyl 4-HO-benzyl Allyl OCH₃ 533 534 2 2,4-Cl₂-benzyl 4-NO₂-benzyl Allyl OCH₃ 562 563 3 2,4-Cl₂-benzyl 2,4-F₂-benzyl Allyl OCH₃ 553 554 4 2,4-Cl₂-benzyl 4-Cl-benzyl Allyl OCH₃ 552 553 5 2,4-Cl₂-benzyl 2,2-bisphenylethyl Allyl OCH₃ 594 595 6 2,4-Cl₂-benzyl 3-t-Bu-4-HO-benzyl Allyl OCH₃ 590 591 7 2,4-Cl₂-benzyl 4-Me-benzyl Allyl OCH₃ 531 532 8 2,4-Cl₂-benzyl Cyclohexylmethyl Allyl OCH₃ 523 524 9 2,4-Cl₂-benzyl 4-F-benzyl Allyl OCH₃ 535 536 10 2,4-Cl₂-benzyl 2-Cl-benzyl Allyl OCH₃ 552 553 11 2,4-Cl₂-benzyl 2,4-Cl₂-benzyl Allyl OCH₃ 586 587 12 2,4-Cl₂-benzyl Naphth-2-ylmethyl Allyl OCH₃ 567 568 13 2,4-Cl₂-benzyl 4-HO-benzyl Benzyl OCH₃ 583 584 14 2,4-Cl₂-benzyl 4-NO₂-benzyl Benzyl OCH₃ 612 613 15 2,4-Cl₂-benzyl 2,4-F₂-benzyl Benzyl OCH₃ 603 604 16 2,4-Cl₂-benzyl 4-Cl-benzyl Benzyl OCH₃ 602 603 17 2,4-Cl₂-benzyl 2,2-bisphenylethyl Benzyl OCH₃ 644 645 18 2,4-Cl₂-benzyl 3-t-Bu-4-HO-benzyl Benzyl OCH₃ 640 641 19 2,4-Cl₂-benzyl 4-Me-benzyl Benzyl OCH₃ 582 583 20 2,4-Cl₂-benzyl Cyclohexylmethyl Benzyl OCH₃ 574 575 21 2,4-Cl₂-benzyl 4-F-benzyl Benzyl OCH₃ 585 586 22 2,4-Cl₂-benzyl 2-Cl-benzyl Benzyl OCH₃ 602 603 23 2,4-Cl₂-benzyl 2,4-Cl₂-benzyl Benzyl OCH₃ 636 637 24 2,4-Cl₂-benzyl Naphth-2-ylmethyl Benzyl OCH₃ 618 619 25 2,4-Cl₂-benzyl 4-HO-benzyl Allyl OCH₃ 479 480 26 2,4-Cl₂-benzyl 4-NO₂-benzyl Allyl OCH₃ 508 509 27 2,4-Cl₂-benzyl 2,4-F₂-benzyl Allyl OCH₃ 499 500 28 2,4-Cl₂-benzyl 4-Cl-benzyl Allyl OCH₃ 497 498 29 Phenethyl 2,2-bisphenylethyl Allyl OCH₃ 539 540 30 Phenethyl 3-t-Bu-4-HO-benzyl Allyl OCH₃ 535 536 31 Phenethyl 4-Me-benzyl Allyl OCH₃ 477 478 32 Phenethyl Cyclohexylmethyl Allyl OCH₃ 469 470 33 Phenethyl 4-F-benzyl Allyl OCH₃ 481 482 34 Phenethyl 2-Cl₂-benzyl Allyl OCH₃ 497 498 35 Phenethyl 2,4-Cl₂-benzyl Allyl OCH₃ 531 532 36 Phenethyl Naphth-2-ylmethyl Allyl OCH₃ 513 514 37 Phenethyl 4-HO-benzyl Benzyl OCH₃ 529 530 38 Phenethyl 4-NO₂-benzyl Benzyl OCH₃ 558 559 39 Phenethyl 2,4-F₂-benzyl Benzyl OCH₃ 549 550 40 Phenethyl 4-Cl-benzyl Benzyl OCH₃ 547 548 41 Phenethyl 2,2-bisphenylethyl Benzyl OCH₃ 589 590 42 Phenethyl 3-t-Bu-4-HO-benzyl Benzyl OCH₃ 585 586 43 Phenethyl 4-Me-benzyl Benzyl OCH₃ 527 528 44 Phenethyl Cyclohexyl-methyl Benzyl OCH₃ 519 520 45 Phenethyl 4-F-benzyl Benzyl OCH₃ 531 532 46 Phenethyl 2-Cl-benzyl Benzyl OCH₃ 547 548 47 Phenethyl 2,4-Cl₂-benzyl Benzyl OCH₃ 582 583 48 Phenethyl Naphth-2-ylmethyl Benzyl OCH₃ 563 564 49 Phenethyl 4-HO-benzyl Allyl OCH₃ 497 498 50 Phenethyl 4-NO₂-benzyl Allyl OCH₃ 526 527 51 Phenethyl 2,4-F₂-benzyl Allyl OCH₃ 517 518 52 Phenethyl 4-Cl-benzyl Allyl OCH₃ 515 516 53 4-F-phenylethyl 2,2-bisphenylethyl Allyl OCH₃ 557 553 54 4-F-phenylethyl 3-t-Bu-4-HO-benzyl Allyl OCH₃ 553 554 55 4-F-phenylethyl 4-Me-benzyl Allyl OCH₃ 495 496 56 4-F-phenylethyl Cyclohexyl-methyl Allyl OCH₃ 487 488 57 4-F-phenylethyl 4-F-benzyl Allyl OCH₃ 499 500 58 4-F-phenylethyl 2-Cl-benzyl Allyl OCH₃ 515 516 59 4-F-phenylethyl 2,4-Cl₂-benzyl Allyl OCH₃ 549 550 60 4-F-phenylethyl Naphth-2-ylmethyl Allyl OCH₃ 531 532 61 4-F-phenylethyl 4-HO-benzyl Benzyl OCH₃ 547 548 62 4-F-phenylethyl 4-NO-benzyl Benzyl OCH₃ 576 577 63 4-F-phenylethyl 2,4-F₂-benzyl Benzyl OCH₃ 567 568 64 4-F-phenylethyl 4-Cl-benzyl Benzyl OCH₃ 565 566 65 4-F-phenylethyl 2,2-bisphenylethyl Benzyl OCH₃ 607 608 66 4-F-phenylethyl 3-t-Bu-4-HO-benzyl Benzyl OCH₃ 603 604 67 4-F-phenylethyl 4-Me-benzyl Benzyl OCH₃ 545 546 68 4-F-phenylethyl Cyclohexyl-methyl Benzyl OCH₃ 537 538 69 4-F-phenylethyl 4-F-benzyl Benzyl OCH₃ 549 550 70 4-F-phenylethyl 2-Cl-benzyl Benzyl OCH₃ 565 566 71 4-F-phenylethyl 2,4-Cl₂-benzyl Benzyl OCH₃ 599 600 72 4-F-phenylethyl Naphth-2-yl-methyl Benzyl OCH₃ 581 582 73 4-F-phenylethyl 4-HO-benzyl Allyl OCH₃ 509 510 74 4-F-phenylethyl 4-NO₂-benzyl Allyl OCH₃ 538 539 75 4-F-phenylelhyl 2,4-F₂-benzyl Allyl OCH₃ 529 530 76 4-F-phenylethyl 4-Cl-benzyl Allyl OCH₃ 527 523 77 4-MeO-phenylethyl 2,2-bisphenylethyl Allyl OCH5 569 570 78 4-MeO-phenylethyl 3-t-Bu-4-HO-benzyl Allyl OCH₃ 565 566 79 4-MeO-phenylethyl 4-Me-benzyl Allyl OCH₃ 507 508 80 4-MeO-phenylethyl Cyclohexyl-methyl Allyl OCH₃ 499 500 81 4-MeO-phenylethyl 4-F-benzyl Allyl OCH₃ 511 512 82 4-MeO-phenylethyl 2-Cl-benzyl Allyl OCH₃ 527 528 33 4-MeO-phenylethyl 2,4-Cl₂-benzyl Allyl OCH₃ 561 562 84 4-MeO-phenylethyl Naphth-2-ylmethyl Allyl OCH₃ 543 544 85 4-MeO-phenylethyl 4-HO-benzyl Benzyl OCH₃ 559 560 86 4-MeO-phenylelhyl 4-NO₂-benzyl Benzyl OCH₃ 588 589 87 4-MeO-phenylethyl 2,4-F₂-benzyl Benzyl OCH₃ 579 580 88 4-MeO-phenylethyl 4-Cl-benzyl Benzyl OCH₃ 577 578 39 4-MeO-phenylethyl 2,2-bisphenylethyl Benzyl OCH₃ 619 620 90 4-MeO-phenylelhyl 3-t-Bu-4-HO-benzyl Benzyl OCH₃ 615 616 91 4-MeO-phenylethyl 4-Me-benzyl Benzyl OCH₃ 557 558 92 4-MeO-phenylethyl Cyclohexylmethyl Benzyl OCH₃ 549 550 93 4-MeO-phenylethyl 4-F-benzyl Benzyl OCH₃ 561 562 94 4-MeO-phenylethyl 2-Cl-benzyl Benzyl OCH₃ 577 578 95 4-MeO-phenylethyl 2,4-Cl-benzyl Benzyl OCH₃ 612 613 96 4-MeO-phenylethyl Naphth-2-ylmethyl Benzyl OCH₃ 593 594 97 Isoamyl 4-HO-benzyl Styrylmethyl OCH₃ 521 522 98 Isoamyl 4-NO₂-benzyl Styrylmethyl OCH₃ 550 551 99 Isoamyl 2,4-F₂-benzyl Styrylmethyl OCH₃ 541 542 100 Isoamyl 4-Cl-benzyl Styrylmethyl OCH₃ 539 540 101 Isoamyl 2,2-bisphenylethyl Styrylmethyl OCH₃ 561 582 102 Isoamyl 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 497 498 103 Isoamyl 4-Me-benzyl Styrylmethyl OCH₃ 519 520 104 Isoamyl Cyclohexylmethyl Slyrylmethyl OCH₃ 511 512 105 Isoamyl 4-F-benzyl Styrylmethyl OCH₃ 523 524 106 Isoamyl 2-Cl-benzyl Styrylmethyl OCH₃ 539 540 107 Isoamyl 2,4-Cl₂-benzyl Styrylmethyl OCH₃ 574 575 108 Isoamyl Naphth-2-ylmethyl Styrylmethyl OCH₃ 555 556 109 Isoamyl 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 563 564 110 Isoamyl 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 592 593 111 Isoamyl 2,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 583 584 112 Isoamyl 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 582 583 113 Isoamyl 2,2-bisphenylethyl 2,6-Cl₂-benzyl OCH₃ 624 625 114 Isoamyl 3-t-Bu-4-HO-benzy 2,6-Cl₂-benzyl OCH₃ 540 541 115 Isoamyl 4-Me-benzyl 2,6-Cl₂-benzyl OCH₃ 562 563 116 Isoamyl Cyclohexylmethyl 2,6-Cl₂-benzyl OCH₃ 554 555 117 Isoamyl 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 565 566 118 Isoamyl 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 582 583 119 Isoamyl 2,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 616 617 120 Isoamyl Naphth-2-ylmethyl 2,6-Cl₂-benzyl OCH₃ 598 599 121 3-MeO-propyl 4-HO-benzyl Styrylmethyl OCH₃ 523 524 122 3-MeO-propyl 4-NO₂-benzyl Styrylmethyl OCH₃ 552 553 123 3-MeO-propyl 2,4-F₂-benzyl Styrylmethyl OCH₃ 543 544 124 3-MeO-propyl 4-Cl-benzyl Styrylmethyl OCH₃ 541 542 125 3-MeO-propyl 2,2-bisphenylethyl Styrylmethyl OCH₃ 583 584 126 3-MeO-propyl 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 499 500 127 3-MeO-propyl 4-Me-benzyl Styrylmethyl OCH₃ 521 522 128 3-MeO-propyl Cyclohexyl-methyl Styrylmethyl OCH₃ 513 514 129 3-MeO-propyl 4-F-benzyl Styrylmethyl OCH₃ 525 526 130 3-MeO-propyl 2-Cl-benzyl Styrylmethyl OCH₃ 541 542 131 3-MeO-propyl 2,4-Cl₂-benzyl Styrylmethyl OCH₃ 575 576 132 3-MeO-propyl Naphth-2-ylmethyl Styrylmethyl OCH₃ 557 558 133 3-MeO-propyl 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 566 566 134 3-MeO-propyl 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 594 595 135 3-MeO-propyl 2,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 585 586 136 3-MeO-propyl 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 584 585 137 3-MeO-propyl 2,2-bisphenylethyl 2,6-Cl₂-benzyl OCH₃ 626 627 138 3-MeO-propyl 3-t-Bu-4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 541 542 139 3-MeO-propyl 4-Me-benzyl 2,6-Cl₂-benzyl OCH₃ 563 564 140 3-MeO-propyl Cyclohexyl-methyl 2,6-Cl₂-benzyl OCH₃ 556 557 141 3-MeO-propyl 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 567 563 142 3-MeO-propyl 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 534 585 143 3-MeO-propyl 2,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 618 619 144 3-MeO-propyl Naphth-2-ylmethyl 2,6-Cl₂-benzyl OCH₃ 600 601 145 4-MeO-phenylethyl 4-HO-benzyl Styrylmethyl OCH₃ 585 586 146 4-MeO-phenylethyl 4-NO₂-benzyl Styrylmethyl OCH₃ 614 615 147 4-MeO-phenylethyl 2,4-F₂-benzyl Styrylmethyl OCH₃ 605 606 148 4-MeO-phenylethyl 4-Cl-benzyl Styrytmethyl OCH₃ 603 604 149 4-MeO-phenylethyl 2,2-bisphenylethyl Styrylmethyl OCH₃ 645 646 150 4-MeO-phenylethyl 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 561 562 151 4-MeO-phenylethyl 4-Me-benzyl Styrylmethyl OCH₃ 583 584 152 4-MeO-phenylethyl Cyclohexyl-methyl Styrylmethyl OCH₃ 575 576 153 4-MeO-phenylethyl 4-F-benzyl Styrylmethyl OCH₃ 687 688 154 4-MeO-phenylethyl 2-Cl-benzyl Styrylmethyl OCH₃ 603 604 155 4-MeO-phenylethyl 2,4-Cl₂-benzyl Styrylmethyl OCH₃ 638 639 156 4-MeO-phenylethyl Naphth-2-ylmethyl Styrylmethyl OCH₃ 619 620 157 4-MeO-phenylethyl 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 628 629 158 4-MeO-phenylethyl 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 657 658 159 4-MeO-phenylethyl 2,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 648 649 160 4-MeO-phenylethyl 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 646 647 161 4-MeO-phenylethyl 2,2-bisphenylethyl 2.6-Cl₂-benzyl OCH₃ 688 689 162 4-MeO-phenylethyl 3-t-Bu-4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 604 605 163 4-MeO-phenylethyl 4-Me-benzyl 2,6-Cl₂-benzyl OCH₃ 626 627 164 4-MeO-phenylethyl Cyclohexylmethyl 2,6-Cl₂-benzyl OCH₃ 618 619 165 4-MeO-phenylethyl 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 630 631 166 4-MeO-phenylethyl 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 646 647 167 4-MeO-phenylethyl 2,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 680 681 168 4-MeO-phenylethyl Naphth-2-ylmethyl 2,6-Cl₂-benzyl OCH₃ 662 663 169 Tetrahydrofuran- 4-HO-benzyl Styrytmethyl OCH₃ 535 536 2-ylmethyl 170 Tetrahydrofuran- 4-NO₂-benzyl Styrytmethyl OCH₃ 564 565 2-ylmethyl 171 Tetrahydrofuran- 2,4-F₂-benzyl Styrylmethyl OCH₃ 555 556 2-ylmethyl 172 Tetrahydrofuran- 4-Cl-benzyl Styrylmethyl OCH₃ 553 554 2-ylmethyl 173 Tetrahydrofuran- 2,2-bisphenylelhyl Styrylmethyl OCH₃ 595 596 2-ylmethyl 174 Tetrahydrofuran- 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 511 512 2-ylmethyl 175 Tetrahydrofuran- 4-Me-benzyl Styrylmethyl OCH₃ 533 534 2-ylmethyl 176 Tetrahydrofuran- Cyclohexyl-methyl Styrylmethyl OCH₃ 525 526 2-ylmethyl 177 Tetrahydroluran- 4-F-benzyl Styrylmethyl OCH₃ 537 538 2-ylmethyl 178 Tetrahydrofuran- 2-Cl-benzyl Styrytmethyl OCH₃ 553 554 2-ylmethyl 179 Tetrahydrofuran- 2,4-Cl₂-benzyl Styrylmethyl OCH₃ 588 589 2-ylmethyl 180 Tetrahydrofuran- Naphth-2-ylmethyl Styrylmethyl OCH₃ 569 570 2-ylmethyl 181 Tetrahydroturan- 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 577 578 2-ylmethyl 182 Tetrahydrofuran- 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 606 607 2-ylmethyl 183 Tetrahydrofuran- 2,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 597 598 2-ylmethyl 184 Tetrahydrofuran- 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 596 597 2-ylmethyl 185 Tetrahydrofuran- 2,2-bisphenylethyl 2,6-Cl₂-benzyl OCH₃ 638 639 2-ylmethyl 186 Tetrahydrofuran- 3-t-Bu-4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 553 554 2-ylmethyl 187 Tetrahydrofuran- 4-Me-benzyl 2,6-Cl₂-benzyl OCH₃ 575 576 2-ylmethyl 188 Tetrahydrofuran- Cyclohexyl-methyl 2,6-Cl₂-benzyl OCH₃ 568 569 2-ylmethyl 180 Tetrahydrofuran- 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 579 580 2-ylmethyl 190 Tetrahydrofuran- 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 596 597 2-ylmethyl 191 Tetrahydrofuran- 2,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 630 631 2-ylmethyl 192 Tetrahydrofuran- Naphth-2-ylmethyl 2,6-Cl₂-benzyl OCH₃ 612 613 2-ylmethyl 193 Phenethyl 4-HO-benzyl Methyl (4-Me-phenyl)amino 528 529 194 Phenethyl 4-HO-benzyl Methyl (4-Cl-phenyl)amino 548 549 195 Phenethyl 4-HO-benzyl Methyl Phenylamino 514 515 196 Phenethyl 4-HO-benzyl Methyl ((R)-α-methylbenzyl)amino 542 543 197 Phenethyl 4-HO-benzyl Methyl Benzylamino 528 529 198 Phenethyl 4-HO-benzyl Methyl (4-MeO-phenyl)amino 544 545 199 Phenethyl 4-HO-benzyl Methyl (4-Br-phenyl)amino 592 593 200 Phenethyl 4-HO-benzyl Methyl (4-CF₃-phenyl)amino 532 583 201 Phenethyl 4-HO-benzyl Methyl Pentylamino 508 509 202 Phenethyl 4-HO-benzyl Methyl (2-Phenylethyl)amino 542 543 203 Phenethyl 4-HO-benzyl Methyl (4-MeO-benzyl)amino 558 559 204 Phenethyl 4-HO-benzyl Methyl Cyclohexylamino 520 521 206 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-Me-phenyl)amino 604 605 206 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-Cl-phenyl)amino 624 625 207 2,2-bisphenylethyl 4-MO-benzyl Methyl Phenylamino 590 591 208 2.2-bisphenylethyl 4-HO-benzyl Methyl ((R)-α-methylbenzy1)amino 618 619 209 2,2-bisphenylethyl 4-HO-benzyl Methyl Benzylamino 604 605 210 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-MeO-phenyl)amino 620 621 211 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-Br-phenyl)amino 669 670 212 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-CF₃-phenyl)amino 658 659 213 2,2-bispbenylethyl 4-HO-benzyl Methyl Phenylamino 534 585 214 2,2-bisphenylethyl 4-HO-benzyl Methyl (2-Phenylethyl)amino 618 619 215 2,2-bisphenylethyl 4-HO-benzyl Methyl (4-MeO-benzyl)amino 634 635 216 2,2-bisphenylethyl 4-HO-benzyl Methyl Cyclohexylamino 596 597 217 Phenethyl 3,4-Cl₂-benzyl Methyl (4-Me-phenyl)amino 581 582 218 Phenethyl 3,4-Cl₂-benzyl Methyl (4-Cl-phenyl)amino 601 602 219 Phenethyl 3,4-Cl₂-benzyl Methyl Phenylamino 566 567 220 Phenethyl 3,4-Cl₂-benzyl Methyl ((R)-α-methylbenzyl)amino 595 596 221 Phenethyl 3,4-Cl₂-benzyl Methyl Benzylamino 581 582 222 Phenethyl 3,4-Cl₂-benzyl Methyl (4-MeO-phenyl)amino 597 598 223 Phenethyl 3,4-Cl₂benzyl Methyl (4-Br-phenyl)amino 645 646 224 Phenethyl 3,4-Cl₂-benzyl Methyl (4-CF₃-phenyl)amino 634 635 225 Phenethyl 3,4-Cl₂-benzyl Methyl Pentylamino 561 562 226 Phenethyl 3,4-Cl₂-benzyl Methyl (2-Phenylethyl)amino 595 596 227 Phenethyl 3,4-Cl₂-benzyl Methyl (4-MeO-benzyl)amino 611 612 228 Phenethyl 3,4-Cl₂-benzyl Methyl Cyclohexylamino 573 574 229 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-Me-phenyl)amino 657 658 230 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-Cl-phenyl)amino 677 678 231 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl Phenylamino 643 644 232 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl ((R)-α-methylbenzyl)amino 671 672 233 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl Benzylamino 657 658 234 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-MeO-phenyl)amino 673 674 235 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-Br-phenyl)amino 721 722 236 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-CF₃-phenyl)amino 711 712 237 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl Pentylamino 637 638 238 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (2-Phenylethyl)amino 671 672 239 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl (4-MeO-benzyl)amino 687 688 240 2,2-bisphenylethyl 3,4-Cl₂-benzyl Methyl Cyclohexylamino 649 650 241 Isoamyl 4-HO-benzyl Methyl (4-Me-phenyl)amino 478 479 242 Isoamyl 4-HO-benzyl Methyl (4-Cl-phenyl)amino 498 499 243 Isoamyl 4-HO-benzyl Methyl Phenylamino 464 465 244 Isoamyl 4-HO-benzyl Methyl ((R)-α-methylbenzyl)amino 492 493 245 Isoamyl 4-HO-benzyl Methyl Benzylamino 478 479 246 Isoamyl 4-HO-benzyl Methyl (4-MeO-phenyl)amino 494 495 247 Isoamyl 4-HO-benzyl Methyl (4-Br-phenyl)amino 542 543 248 Isoamyl 4-HO-benzyl Methyl (4-CF₃-phenyl)amino 532 533 249 Isoamyl 4-HO-benzyl Methyl Pentylamino 458 459 250 Isoamyl 4-HO-benzyl Methyl (2-Phenylethyl)amino 492 493 251 Isoamyl 4-HO-benzyl Methyl (4-MeO-benzyl)amino 508 509 252 Isoamyl 4-HO-benzyl Methyl Cyclohexylamino 470 471 253 Isoamyl 4-HO-benzyl Methyl (4-Me-phenyl)amino 554 555 254 Isoamyl 4-HO-benzyl Methyl (4-Cl-phenyl)amino 574 575 255 Isoamyl 4-HO-benzyl Methyl Phenylamino 540 541 256 Isoamyl 4-HO-benzyl Methyl ((R)-α-methylbenzyl)amino 568 569 257 Isoamyl 4-HO-benzyl Methyl Benzylamino 554 555 258 Isoamyl 4-HO-benzyl Methyl (4-MeO-phenyl)amino 570 571 259 Isoamyl 4-HO-benzyl Methyl (4-Br-phenyl)amino 619 620 260 Isoamyl 4-HO-benzyl Methyl (4-CF₃-phenyl)amino 603 609 261 Isoamyl 4-HO-benzyl Methyl Pentylamino 534 535 262 Isoamyl 4-HO-benzyl Methyl (2-Phenylethyl)amino 568 569 263 Isoamyl 4-HO-benzyl Methyl (4-MeO-benzyl)amino 584 585 264 Isoamyl 4-HO-benzyl Methyl Cyclohexylamino 548 547 265 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Me-phenyl)amino 526 527 266 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Cl-phenyl)amino 546 547 267 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Phenylamino 512 513 268 4-methylbenzyl 3,4-Cl₂-benzyl Methyl ((R)-α-methylbenzyl)amino 540 541 269 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Benzylamino 526 527 270 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-MeO-phenyl)amino 542 543 271 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Br-phenyl)amino 591 592 272 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-CF₃-phenyl)amino 580 581 273 4-methylbenzyl 3.4-Cl₂-benzyl Methyl Pentylamino 506 507 274 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (2-Phenylethyl)amino 540 541 275 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-MeO-benzyl)amino 556 557 276 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Cyclohexylamino 518 519 277 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Me-phenyl)amino 602 603 276 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Cl-phenyl)amino 622 623 279 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Phenylamino 588 589 280 4-methylbenzyl 3,4-Cl₂-benzyl Methyl ((R)-α-methylbenzyl)amino 616 617 281 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Benzylamino 602 603 282 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-MeO-phenyl)amino 618 619 283 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-Br-phenyl)amino 667 668 284 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-CF₃-phenyl)amino 656 657 285 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Pentylamino 582 583 286 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (2-Phenylethyl)amino 616 617 287 4-methylbenzyl 3,4-Cl₂-benzyl Methyl (4-MeO-benzyl)amino 632 633 288 4-methylbenzyl 3,4-Cl₂-benzyl Methyl Cyclohexylamino 594 595 289 Naphth-1-ylmethyl 4-HO-benzyl Methyl (N-Cbz-3-Indoleethyl)amino 751 752 290 Naphth-1-ylmethyl 4-HO-benzyl Methyl (Naphth-2-ylmethyl)amino 614 615 291 Naphth-1-ylmethyl 4-HO-benzyl Methyl (2-Phenylethyl)amino 578 579 292 Napnth-1-ylmethyl 4-HO-benzyl Methyl [2-(4-MeO-phenyl)ethyl]amino 608 609 293 Naphlh-1-ylmethyl 4-HO-benzyl Methyl (3-CF₃-benzyl)amino 632 633 294 Naphth-1-ylmethyl 4-HO-benzyl Methyl (4-MeO-benzyl)amino 594 595 295 Naphth-1-ylmethyl 4-HO-benzyl Methyl (4-F-phenylethyl)amino 596 597 296 Naphth-1-ylmethyl 4-HO-benzyl Methyl (3,4-Cl₂-benzyl)amino 633 634 297 Naphth-1-ylmethyl 4-HO-benzyl Methyl (2-HO-ethyl)amino 518 519 298 Naphth-1-ylmethyl 4-HO-benzyl Methyl (3-MeO-propyl)amino 546 547 299 Naphth-1-ylmethyl 4-HO-benzyl Methyl (Tetrahydrofuran-2-ylmethyl) 558 559 amino 300 Naphth-1-ylmethyl 4-HO-benzyl Methyl (cyclohexylmethyl)amino 570 571 301 Naphth-1-ylmethyl 4-HO-benzyl Propyl (N-Cbz-3-lndoleethyl)amino 779 780 302 Naphth-1-ylmethyl 4-HO-benzyl Propyl (Naphth-2-ylmethyl)amino 642 643 303 Naphth-1-ylmethyl 4-HO-benzyl Propyl (2-Phenylethyl)amino 606 607 304 Naphth-1-ylmethyl 4-HO-benzyl Propyl [2-(4-MeO-phenyl)ethyl]amino 636 637 305 Naphth-1-ylmethyl 4-HO-benzyl Propyl (3-CF₃-benzyl)amino 660 661 306 Naphth-1-ylmethyl 4-HO-benzyl Propyl (4-MeO-benzyl)amino 622 623 307 Naphth-1-ylmethyl 4-HO-benzyl Propyl (4-F-phenylethyl)amino 624 625 308 Naphth-1-ylmethyl 4-HO-benzyl Propyl (3,4-Cl₂-benzyl)amino 661 662 309 Naphth-1-ylmethyl 4-HO-benzyl Propyl (2-HO-ethyl)amino 546 547 310 Naphth-1-ylmethyl 4-HO-benzyl Propyl (3-MeO-propyl)amino 574 575 311 Naphth-1-ylmethyl 4-HO-benzyl Propyl (Tetrahydrofuran-2-ylmethyl) 586 587 amino 312 Naphth-1-ylmethyl 4-HO-benzyl Propyl (cyclohexylmethyl)amino 598 599 313 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (N-Cbz-3-Indoleethyl)amino 771 772 314 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (Naphth-2-ylmethyl)amino 634 635 315 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (2-Phenylethyl)amino 598 599 316 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl [2-(4-MeO-phenyl)ethyl]amino 628 629 317 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (3-CF₃-benzyl)amino 652 653 318 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl {4-MeO-benzyl)amino 614 615 319 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (4-F-phenylethyl)amino 616 617 320 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (3,4-Cl₂-benzyl)amino 653 654 321 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (2-HO-ethyl)amino 538 539 322 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (3-MeO-propyl)amino 566 567 323 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (Tetrahydrofuran-2-ylmethyl) 578 579 amino 324 Naphth-1-ylmethyl 3,4-F₂-benzyl Methyl (cyclohexylmethyl)amino 590 591 325 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (N-Cbz-3-Indoleethyl)amino 799 800 326 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (Naphth-2-ylmethyl)amino 662 663 327 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (2-Phenylethyl)amino 626 627 328 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl [2-(4-MeO-phenyl)ethyl]amino 656 657 329 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (3-CF₃-benzyl)amino 680 681 330 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (4-MeO-benzyl)amino 642 643 331 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (4-F-phenylethyl)amino 644 645 332 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (3,4-Cl₂-benzyl)amino 661 682 333 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (2-HO-ethyl)amino 566 567 334 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (3-MeO-propyl)amino 594 595 335 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (Tetrahydrofuran-2-ylmethyl) 606 607 amino 336 Naphth-1-ylmethyl 3,4-F₂-benzyl Propyl (cyclohexylmethyl)amino 618 619 337 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (N-Cbz-3-Indoleethyl)amino 811 812 338 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (Naphth-2-ylmethyl)amino 674 675 339 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (2-Phenylethyl)amino 638 639 340 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl [2-(4-MeO-phenyl)ethyl]amino 668 669 341 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (3-CF₃-benzyl)amino 692 693 342 Naphth-1-ylmethyl 4-biphenylylmethyl Methvl (4-MeO-benzyl)amino 654 655 343 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (4-F-phenylethyl)amino 656 657 344 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (3,4-Cl₂-benzyl)amino 693 694 345 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (2-HO-ethyl)amino 573 579 346 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (3-MeO-propyl)amino 606 607 347 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (Tetrahydrofuran-2-ylmethyl) 613 619 amino 348 Naphth-1-ylmethyl 4-biphenylylmethyl Methyl (cyclohexylmethyl)amino 630 631 349 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (N-Cbz-3-Indoleethyl)amino 839 840 350 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (Naphth-2-ylmethyl)amino 702 703 351 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (2-Phenylethyl)amino 666 667 352 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl [2-(4-MeO-phenyl)ethyl]amino 696 697 353 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (3-CF₃-benzyl)amino 720 721 354 Naphth-1-ylmethyl 4-biphenylyfmethyl Propyl (4-MeO-benzyl)amino 682 683 355 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (4-F-phenylethyl)amino 684 685 356 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (3,4-Cl₂-benzyl)amino 721 722 357 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (2-HO-ethyl)amino 606 607 358 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (3-MeO-propyl)amino 634 635 359 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (Tetrahydrofuran-2-ylmethyl) 646 647 amino 360 Naphth-1-ylmethyl 4-biphenylylmethyl Propyl (cyclohexylmethyl)amino 658 659 361 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (N-Cbz-3-Indoleethyl)amino 807 808 362 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (Naphth-2-ylmethyl)amino 670 671 363 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (2-Phenylethyl)amino 634 635 364 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl [2-(4-MeO-phenyl)ethyl]amino 664 665 365 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (3-CF₃-benzyl)amino 688 689 366 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (4-MeO-benzyl)amino 650 651 367 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (4-F-phenylethyl)amino 662 653 368 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (3,4-Cl₂-benzyl)amino 669 690 369 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (2-HO-ethyl)amino 574 575 370 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (3-MeO-propyl)amino 602 603 371 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (Tetrahydrofuran-2-ylmethyl) 814 615 amino 372 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl (cyclohexylmethyl)amino 626 627 373 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (N-Cbz-3-Indoleethyl)amino 835 836 374 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (Naphth-2-ylmethyl)amino 698 699 375 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (2-Phenylethyl)amino 662 663 376 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl [2-(4-MeO-phenyl)ethyl]amino 692 693 377 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (3-CF₃-benzyl)amino 716 717 378 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (4-MeO-benzyl)amino 678 679 379 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (4-F-phenylethyl)amino 680 681 380 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (3,4-Cl₂-benzyl)amino 717 718 381 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (2-HO-ethyl)amino 602 603 382 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (3-MeO-propyl)amino 630 631 383 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (Tetrahydrofuran-2-ylmethyl) 642 643 amino 384 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Propyl (cyclohexylmethyl)amino 654 655 385 4-Methoxybenzyl OCH₃ 5-F-benzyl OCH₃ 470 471 386 Naphth-1-ylmethyl 4-HO-benzyl Styrylmethyl OCH₃ 591 592 387 Naphth-1-ylmethyl 4-NO₂-benzyl Styrylmethyl OCH₃ 620 621 388 Naphth-1-ylmethyl 3,4-F₂-benzyl Styrylmethyl OCH₃ 611 612 389 Naphth-1-ylmethyl 4-Cl-benzyl Styrylmethyl OCH₃ 609 610 390 Naphth-1-ylmethyl 4-Phenyl-benzyl Styrylmethyl OCH₃ 651 652 391 Naphth-1-ylmethyl 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 647 648 392 Naphth-1-ylmethyl 4-Methyl-benzyl Styrylmethyl OCH₃ 589 590 393 Naphth-1-ylmethyl Cyclohexylmethyl Styrylmethyl OCH₃ 581 582 394 Naphth-1-ylmethyl 4-F-benzyl Styrylmethyl OCH₃ 593 594 395 Naphthyl-1-ylmethyl 2-Cl-benzyl Styrylmethyl OCH₃ 609 610 396 Naphthyl-1-ylmethyl 3,4-Cl₂-benzyl Styrylmethyl OCH₃ 644 645 397 Naphthyl-1-ylmethyl Naphthyl-1-ylmethyl Styrylmethyl OCH₃ 625 626 398 3,4-Cl₂-benzyl 4-HO-benzyl Styrylmethyl OCH₃ 610 611 399 3,4-Cl₂-benzyl 4-NO₂-benzyl Styrylmethyl OCH₃ 639 640 400 3,4-Cl₂-benzyl 3,4-F₂-benzyl Styrylmethyl OCH₃ 629 630 401 3,4-Cl₂-benzyl 4-Cl-benzyl Styrylmethyl OCH₃ 628 629 402 3,4-Cl₂-benzyl 4-Phenyl-benzyl Styrylmethyl OCH₃ 670 671 403 3,4-Cl₂-benzyl 3-t-Bu-4-HO-benzyl Styrylmethyl OCH₃ 666 667 404 3,4-Cl₂-benzyl 4-Methyl-benzyl Styrylmethyl OCH₃ 608 609 400 3,4-Cl₂-benzyl Cyclohexylmethyl Styrylmethyl OCH₃ 600 601 406 3,4-Cl₂-benzyl 4-F-benzyl Styrylmethyl OCH₃ 611 612 407 3,4-Cl₂-benzyl 2-Cl-benzyl Styrylmethyl OCH₃ 628 629 408 3,4-Cl₂-benzyl 3,4-Cl₂-benzyl Styrylmethyl OCH₃ 662 663 409 3,4-Cl₂-benzyl Naphthyl-1-ylmethyl Styrylmethyl OCH₃ 644 645 410 Naphthyl-1-ylmethyl 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 634 635 411 Naphthyl-1-ylmethyl 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 663 064 412 Naphthyl-1-ylmethyl 3,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 654 655 413 Naphthyl-1-ylmethyl 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 652 653 414 Naphthyl-1-ylmethyl 4-Phenyl-benzyl 2,6-Cl₂-benzyl OCH₃ 694 695 415 Naphthyl-1-ylmethyl 3-t-Bu-4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 690 691 416 Naphthyl-1-ylmethyl 4-Methyl-benzyl 2,6-Cl₂-benzyl OCH₃ 632 633 417 Naphthyl-1-ylmethyl Cyclohexylmethyl 2,6-Cl₂-benzyl OCH₃ 624 625 418 Naphthyl-1-ylmethyl 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 636 637 419 Naphthyl-1-ylmethyl 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 652 653 420 Naphthyl-1-ylmethyl 3,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 686 687 421 Naphthyl-1-ylmethyl Naphthyl-1-ylmethyl 2,6-Cl₂-benzyl OCH₃ 668 669 422 3,4-Cl₂-benzyl 4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 652 653 423 3,4-Cl₂-benzyl 4-NO₂-benzyl 2,6-Cl₂-benzyl OCH₃ 681 682 424 3,4-Cl₂-benzyl 3,4-F₂-benzyl 2,6-Cl₂-benzyl OCH₃ 672 673 425 3,4-Cl₂-benzyl 4-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 671 672 426 3,4-Cl₂-benzyl 4-Phenyl-benzyl 2,6-Cl₂-benzyl OCH₃ 712 713 427 3,4-Cl₂-benzyl 3-t-Bu-4-HO-benzyl 2,6-Cl₂-benzyl OCH₃ 708 709 428 3,4-Cl₂-benzyl 4-Methyl-benzyl 2,6-Cl₂-benzyl OCH₃ 650 651 429 3,4-Cl₂-benzyl Cyclohexylmethyl 2,6-Cl₂-benzyl OCH₃ 642 643 430 3,4-Cl₂-benzyl 4-F-benzyl 2,6-Cl₂-benzyl OCH₃ 654 655 431 3,4-Cl₂-benzyl 2-Cl-benzyl 2,6-Cl₂-benzyl OCH₃ 671 672 432 3,4-Cl₂-benzyl 3,4-Cl₂-benzyl 2,6-Cl₂-benzyl OCH₃ 705 706 433 3,4-Cl₂-benzyl Naphthyl-1-ylmethyl 2,6-Cl₂-benzyl OCH₃ 686 687 434 2-Piperidin- (S)-4-HO-benzyl Methyl Benzylamino 535 536 1-yl-ethyl 435 3,4-Cl₂-benzyl (S)-4-HO-benzyl Methyl 2-Piperidin-1-yl-ethylamino 604 605 436 3,4-Cl₂-benzyl (S)-4-HO-benzyl Methyl 2-(1-Methyl-pyrrolidin- 604 605 2-yl)-ethylamino 437 3-Pyridylmethyl (S)-4-HO-benzyl Methyl 3,4-Cl₂-benzylamino 583 584 438 2-Morpholin- (S)-4-HO-benzyl Methyl 3,4-Cl₂-benzylamino 606 607 4-yl-ethyl 439 3,4-Cl₂-benzyl (S)-4-HO-benzyl Methyl 3-Pyridylmethylamino 563 584 440 3,4-Cl₂-benzyl (S)-4-HO-benzyl Methyl 2-Morpholin-4-yl-ethylamino 606 607 441 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 3-Imidazol-1-yl-propylamino 582 583 442 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-Aminophenethylamino 593 594 443 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 3-Pyridylmethylamino 565 566 444 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 2-(3-Pyridylethyl)amino 579 580 445 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-Pyridylmethylamino 565 566 446 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Benzyloxycarbonylamino 622 623 447 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-F-benzylamino 582 583 448 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-CO₂H-benzylamino 608 609 449 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-CF₃-benzylamino 632 633 450 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl (S)-alpha-methylbenzylamino 578 579 451 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl (R)-alpha-methylbenzylamino 578 579 452 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 2-F-benzylamino 582 583 453 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 2,3-Dimethoxybenzylamino 624 625 454 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Cyanomethylamino 513 514 455 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Phanylhydrazino 565 566 456 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-Aminobenzylamino 579 580 457 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl (S,S){2-[(2-hydroxy-1- 693 694 methyl-2-phenyl-ethyl)-methyl- carbamoyl]-ethyl}-amino 458 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl [4-(1,3-dioxo-1,3- 715 716 dihydro-isoindol-2-ylmethyl)- cyclohexyl]-methylamino 459 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Indan-1-ylamino 590 591 460 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl PhenylGlycine 622 623 461 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 2,6-F₂-benzylamino 600 601 462 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 3-F-benzylamino 582 583 463 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Benzimidazol-2-yl-amino 604 605 464 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Diphenylmethylamino 640 641 465 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Furan-2-yl-methylamino 554 555 466 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-Dimethylamino-benzylamino 607 608 467 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Thiofuran-2-yl-methylamino 584 585 468 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-NO₂-benzylamino 609 610 469 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl BnO 565 566 470 4-Methoxy- 4-HO-benzyl Methyl Benzylamino 594 595 naphthyl-1-ylmethyl 471 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Phenethyl 563 564 472 Naphthyl-1-ylmethyl 4-Methoxy-benzyl Methyl Benzylamino 578 579 473 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 4-CF₃-phenylamino 618 619 474 Naphthyl-1-ylmethyl 4-NO₂-benzyl Methyl 4-CF₃-phenylamino 647 648 475 Naphthyl-1-ylmethyl 4-NO₂-benzyl Methyl Benzylamino 593 594 476 Benzyl Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 574 575 477 Thiofuran-2- Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 594 595 yl-methylamino 476 4-Dimethylamino-benzyl Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 617 618 479 Phenethyl Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 588 589 480 8-Quinoline-1yl-methyl 4-HO-benzyl Methyl Benzylamino 565 566 481 4-Pyridylmethyl Naphthyl-1-ylmethyl Benzyl OCH₃ 550 551 482 3,4-Dimethoxybenzyl Naphthyl-1-ylmethyl Benzyl OCH₃ 609 610 483 3,4-Dimethoxy-phenethyl Naphthyl-1-ylmethyl Benzyl OCH₃ 623 624 484 Thiofuran-2- Naphthyl-1-ylmethyl Benzyl OCH₃ 569 570 yl-methylamino 485 Naphthyl-1-ylmethyl 3-Pyridylmethyl Methyl Benzylamino 549 550 486 Naphthyl-1-ylmethyl Pentafluorobenzyl Methyl Benzylamino 638 639 487 Naphthyl-1-ylmethyl 3-F-4-HO-benzy! Methyl Benzylamino 582 583 488 4-F-phenethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 598 599 489 4-Methoxyphenethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 610 611 490 3,4-Dimethoxy-phenethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 640 641 491 Naphthyl-1-ylmethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 616 617 492 3,4-Dimethoxybenzyl Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 634 635 493 3,4-Dimethoxy-phenethyl Naphthyl-1-ylmethyl 4-CN-benzyl OCH₃ 648 649 494 4-Quinoline-1yl-methyl 4-HO-benzyl Methyl Benzylamino 565 566 495 2-Pyridylmethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 567 568 496 3-Pyridylmethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 567 568 497 3,4-Dimethoxybenzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 626 627 498 4-Methyl-benzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 580 581 499 Thiofuran-2- 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 572 573 yl-methylamino 500 4-CF₃-benzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 634 635 501 2,6-F₂-benzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 602 603 502 4-F-benzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 584 585 503 Thiofuran-2-yl-ethyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 586 587 504 3,4-Cl₂-benzyl 4-Methyl-benzyl Methyl 4-CF₃-phenylamino 634 635 505 4-CO₂H-benzyl 4-HO-benzyl Methyl Benzylamino 558 559 506 Naphthyl-1-ylmethyl 3-t-Bu-4-HO-benzyl Methyl Benzylamino 620 621 507 Naphthyl-1-ylmethyl 3,4-(OH)2-benzyl Methyl Benzylamino 580 581 508 2-F-benzyl 4-HO-benzyl Methyl Benzylamino 532 533 509 3-F-benzyl 4-HO-benzyl Methyl Benzylamino 532 533 510 4-F-benzyl 4-HO-benzyl Methyl Benzylamino 532 533 511 2,4-F₂-benzyl 4-HO-benzyl Methyl Benzylamino 550 551 512 2,6-F₂-benzyl 4-HO-benzyl Methyl Benzylamino 550 551 513 2,5-F₂-benzyl 4-HO-benzyl Methyl Benzylamino 550 551 514 3-CF₃-benyl 4-HO-benzyl Methyl Benzylamino 582 583 515 4-CF₃-benyl 4-HO-benzyl Methyl Benzylamino 582 583 516 3,4,5-F₃-benyl 4-HO-benzyl Methyl Benzylamino 553 569 517 2-Cl-benzyl 4-HO-benzyl Methyl Benzylamino 548 549 518 3-Cl-benzyl 4-HO-benzyl Methyl Benzylamino 548 549 519 2,4-Cl₂-benzyl 4-HO-benzyl Methyl Benzylamino 582 583 520 (S)-Methylphenyl 4-HO-benzyl Methyl Benzylamino 528 529 521 (R)-Methylphenyl 4-HO-benzyl Methyl Benzylamino 528 529 522 4-Methyl-benzyl 4-HO-benzyl Methyl Benzylamino 528 529 523 4-Methoxybenzyl 4-HO-benzyl Methyl Benzylamino 544 545 524 3,4-Dimethoxybenzyl 4-HO-benzyl Methyl Benzylamino 574 575 525 Furan-2-yl-methylamino 4-HO-benzyl Methyl Benzylamino 504 505 526 (R)-Methylnaphthyl- 4-HO-benzyl Methyl Benzylamino 573 579 1-ylmethyl 527 (S)-Methylnaphthyl- 4-HO-benzyl Methyl Benzylamino 578 579 1-ylmethyl 528 Naphthyl-1-ylmethyl 3-Oxy-pyridin-1- Methyl Benzylamino 565 566 ylmethyl 529 (R)-alpha-methylbenzyl 4-HO-benzyl Methyl Benzylamino 578 579 530 Naphthyl-2-ylmethyl 4-HO-benzyl Methyl Benzylamino 564 565 531 4-F-naphthyl-ylmethyl 4-HO-benzyl Methyl Benzylamino 582 583 532 2-Methoxybenzyl 4-HO-benzyl Methyl Benzylamino 544 545 533 4-Cl-benzyl 4-HO-benzyl Methyl Benzylamino 543 549 534 3,4-Cl₂-benzyl 4-HO-benzyl Methyl Benzylamino 582 583 535 2-CF₃Obenzyl 4-HO-benzyl Methyl Benzylamino 598 599 536 2-CF₃Sbenzyl 4-HO-benzyl Methyl Benzylamino 614 615 537 2-CF₃-benzyl 4-HO-benzyl Methyl Benzylamino 582 583 538 5-Quinoline-1yl-methyl 4-HO-benzyl Methyl Benzylamino 565 566 539 8-Quinoline-1yl-methyl 3-t-Bu-4-HO-benzyl Methyl Benzylamino 621 622 540 8-Quinoline-1yl-methyl 4-NO₂-benzyl Methyl Benzylamino 594 595 541 8-Quinoiine-1yl-methyl (1H-Pyrrol-2-yl)- Methyl Benzylamino 538 539 methyl 542 Naphthyl-1-ylmethyl 4-Benzyloxy- Methyl Benzylamino 697 698 carbonylaminobenzyl 543 2,3-Cl₂-benzyl 4-HO-benzyl Methyl Benzylamino 582 583 544 Pentafluorobenzyl 4-HO-benzyl Methyl Benzylamino 604 605 545 Benzyl 4-HO-benzyl Methyl Benzylamino 514 515 546 Quinoxaline-5yl-methyl 4-HO-benzyl Methyl Benzylamino 566 567 547 8-Quinoiine-1yl-methyl 3-Pyridylmethyl Methyl Benzylamino 550 551 548 8-Quinoline-1yl-methyl Pentafluorobenzyl Methyl Benzylamino 639 640 549 Naphthyl-1-ytmethyl 4-HO-benzyl Methyl Benzylamino(thiourea) 580 581 550 Naphthyl-1-yimethyl 4-Amino-benzyl Methyl Benzylamino 563 564 551 3,4,5-tri-Methoxybenzyl 4-Amino-benzyl Methyl Benzylamino 603 604 552 Naphthyl-1-ylmethyl 4-Pyridylmethyl Methyl Benzylamino 549 550 553 Naphthyl-1-ylmethyl (R)4-HO-phenyl Methyl Benzylamino 550 551 554 2-HO-3-Methoxy-benzyl 4-HO-benzyl Methyl Benzylamino 560 561 555 Naphthyl-1-ylmethyl 3-Nitro-4-HO-benzyl Methyl Benzylamino 609 610 556 Naphthyl-1-ylmethyl 4-CO₂H-CH2-O-benzyl Methyl Benzylamino 622 623 557 Naphthyl-1-ylmethyl 1-Naphtoylamino-methyl Methyl Benzylamino 641 642 558 Naphthyl-1-ylmethyl 4-Oxy-pyridylmethyl Methyl Benzylamino 565 566 559 4-F-alpha-methylbenzyl 4-HO-benzyl Methyl Benzylamino 546 547 560 Naphthyl-1-ylmethyl Benzoylaminoethyl Methyl Benzylamino 605 606 561 8-Quinoline-1yl-methyl 3,4-(OH)₂-benzyl Methyl Benzylamino 581 582 562 4-N,N-Dimethylamino- 4-HO-benzyl Methyl Benzylamino 557 558 benzyl 563 Naphthyl-1-ylmethyl (R)4-F-benzyl Methyl Benzylamino 609 610 564 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl 2-Chloroethylamino 536 537 565 Naphthyl-1-ylmethyl 4-HO-phenethyl Methyl Benzylamino 578 579 566 4-F-benzyl 3-F,4-HO-benzyl Methyl Benzylamino 550 551 567 2,4-F₂-benzyl 3-F,4-HO-benzyl Methyl Benzylamino 568 569 568 3-CF₃benzyl (R)4-HO-benzyl Methyl Benzylamino 568 569 569 (S)-Methylnaphthyl- (R)4-HO-phenyl Methyl Benzylamino 514 515 1-ylmethyl 570 (R)-Methylnaphthyl- (R)4-HO-phenyl Methyl Benzylamino 514 515 1-ylmethyl 571 2,3,6-F₃-benzyl (R)4-HO-phenyl Methyl Benzylamino 554 555 572 3-F-benzyl (R)4-HO-phenyl Methyl Benzylamino 518 519 573 4-Cl-benzyl (R)4-HO-phenyl Methyl Benzylamino 534 535 574 3-Cl-benzyl (R)4-HO-phenyl Methyl Benzylamino 534 535 575 2-Cl-benzyl (R)4-HO-phenyl Methyl Benzylamino 534 535 576 3,4-Cl₂-benzyl (R)4-HO-phenyl Methyl Benzylamino 568 569 577 3-CF₃O-benzyl (R)4-HO-phenyl Methyl Benzylamino 584 585 578 4-F-benzyl (R)4-HO-phenyl Methyl Benzylamino 518 519 579 2,4-F₂-benzyl (R)4-HO-phenyl Methyl Benzylamino 536 537 580 3-(2-Chloro-ethyl)- 4-HO-benzyl Methyl Benzylamino 634 635 ureido]-benzyl 581 3-Aminobenzyl 4-HO-benzyl Methyl Benzylamino 529 530 582 3-N-Methylaminobenzyl 4-HO-benzyl Methyl Benzylamino 543 544 583 3-N,N- 4-HO-benzyl Methyl Benzylamino 557 558 Dimethylaminobenzyl 584 1H-Benzoimidazol- 4-HO-benzyl Methyl Benzylamino 554 555 4-ylmethyl 585 2-HO-benzyl 4-HO-benzyl Methyl Benzylamino 530 531 586 2-Pyridylmethyl 4-HO-benzyl Methyl Benzylamino 515 516 587 4-Pyridylmethyl 4-HO-benzyl Methyl Benzylamino 515 516 588 8-quinolin-2-ylmethyl 4-HO-benzyl Methyl Benzylamino 565 566 589 8-Benzofuran-4-ylmethyl 4-HO-benzyl Methyl Benzylamino 554 555 590 Naphthyl-1-ylmethyl 4-HO-phenyl Methyl Benzylamino 550 551 591 4-F-benzyl 4-HO-phenyl Methyl Benzylamino 518 519 592 2,4-F₂-benzyl 4-HO-phenyl Methyl Benzylamino 536 537 593 (R)-Toluylmethyl 4-HO-benzyl Methyl Benzylamino 542 543 594 (S)-Toluylmethyl 4-HO-benzyl Methyl Benzylamino 542 543 595 1,2,3,4-tetrahydra- 4-HO-benzyl Methyl Benzylamino 554 555 naphthalen-2-yl 596 Naphthyl-1-ylmethyl 3.4-Dimethoxybenzyl Methyl Benzylamino 608 609 597 2-Dimethylamino-6- 4-HO-benzyl Methyl Benzylamino 575 576 F-benzyl 598 2-Dimethylaminobenzyl 4-HO-benzyl Methyl Benzylamino 557 558 599 Naphthyl-1-ylmethyl 4-HO-benzyl Methyl Benzylamino 573 574 600 4-F-2-CF₃-benzyl 4-HO-benzyl Methyl Benzylamino 599 600 601 4-Cl-2-Dimethylaminobenzyl 4-HO-benzyl Methyl Benzylamino 591 592 602 3-N,N-Ethylmethyllamino- 4-HO-benzyl Methyl Benzylamino 571 572 benzyl 603 3-Diethylaminobenzyl 4-HO-benzyl Methyl Benzylamino 585 586 604 4-Cl-3-Dimethylaminobenzyl 4-HO-benzyl Methyl Benzylamino 591 592 605 4-F-2-Dimethylaminobenzyl 4-HO-benzyl Methyl Benzylamino 575 576 606 3,5-(CH₃)₂-2- 4-HO-benzyl Methyl Benzylamino 585 586 Dimethylamino-benzyl 607 3-(CH₃)-2- 4-HO-benzyl Methyl Benzylamino 571 572 Dimethylaminobenzyl 608 6-(CH₃)-2- 4-HO-benzyl Methyl Benzylamino 571 572 Dimethylaminobenzyl 609 3,4-F₂-2- 4-HO-benzyl Methyl Benzylamino 593 594 Dimethylaminobenzyl

TABLE 2B THE [4,4,0] REVERSE TURN MIMETICS LIBRARY

Mol. M + H No MOLSTRUCTURE Weight (MS) 802

480 481 803

430 431 804

416 417 805

464 465 806

430 431 807

430 431 808

448 449 809

416 417 810

431 432 811

446 447 812

450 451 813

515 516 814

582 583 815

532 533 816

518 519 817

566 567 818

532 533 819

532 533 820

550 551 821

518 519 822

534 535 823

548 549 824

552 553 825

617 618 826

542 543 827

492 493 828

478 479 829

526 527 830

492 493 831

492 493 832

510 511 833

478 479 834

494 495 835

508 509 836

512 513 837

577 578 838

468 469 839

516 517 840

482 483 841

482 483 842

468 469 843

484 485 844

498 499 845

502 503 846

567 568 847

508 509 848

458 459 849

444 445 850

492 493 851

458 459 852

458 459 853

476 477 854

444 445 855

460 461 856

474 475 857

478 479 858

543 544 859

494 495 860

444 445 861

430 431 862

478 479 863

444 445 864

444 445 865

462 463 866

430 431 867

446 447 868

460 461 869

464 465 870

529 530 871

558 559 872

508 509 873

494 495 874

542 543 875

508 509 876

508 509 877

526 527 878

494 495 879

510 511 880

524 525 881

528 529 882

593 594 883

432 433 884

480 481 885

446 447 886

446 447 887

464 465 888

432 433 889

447 448 890

462 463 891

466 467 892

531 532 893

558 559 894

508 509 895

494 495 896

542 543 897

508 509 898

508 509 899

526 527 900

494 495 901

510 511 902

524 525 903

528 529 904

593 594 905

544 545 906

494 495 907

480 481 908

528 529 909

494 495 910

494 495 911

512 513 912

480 481 913

496 497 914

510 511 915

514 515 916

579 580 917

464 465 918

450 451 919

498 499 920

464 465 921

464 465 922

482 483 923

450 451 924

466 467 925

480 481 926

484 485 927

549 550 928

480 481 929

430 431 930

416 417 931

464 465 932

430 431 933

430 431 934

448 449 935

416 417 936

431 432 937

446 447 938

450 451 939

515 516 940

504 505 941

454 455 942

440 441 943

488 489 944

454 455 945

454 455 946

472 473 947

440 441 948

455 456 949

470 471 950

474 475 951

539 540 952

604 605 953

554 555 954

540 541 955

588 589 956

554 555 957

554 555 958

572 573 959

540 541 960

556 557 961

570 571 962

574 575 963

639 640 964

528 529 965

478 479 966

464 465 967

512 513 968

478 479 969

478 479 970

496 497 971

464 465 972

480 481 973

494 495 974

498 499 975

563 564 976

582 583 977

532 533 978

518 519 979

566 567 980

532 533 981

532 533 982

551 552 983

518 519 984

534 535 985

548 549 986

552 553 987

618 619 988

482 483 989

432 433 990

418 419 991

466 467 992

432 433 993

432 433 994

450 451 995

418 419 996

433 434 997

447 448 998

452 453 999

517 518 1000

548 549 1001

498 499 1002

484 485 1003

532 533 1004

498 499 1005

498 499 1006

516 517 1007

484 485 1008

500 501 1009

514 515 1010

518 519 1011

583 584 1012

532 533 1013

518 519 1014

566 567 1015

532 533 1016

532 533 1017

551 552 1018

518 519 1019

534 535 1020

548 549 1021

552 553 1022

618 619 1023

528 529 1024

478 479 1025

464 465 1026

512 513 1027

478 479 1028

478 479 1029

496 497 1030

464 465 1031

480 481 1032

494 495 1033

498 499 1034

563 564 1035

528 529 1036

478 479 1037

464 465 1038

512 513 1039

478 479 1040

478 479 1041

496 497 1042

464 465 1043

480 481 1044

494 495 1045

498 499 1046

563 564 1047

556 557 1048

506 507 1049

492 493 1050

540 541 1051

506 507 1052

506 507 1053

524 525 1054

492 493 1055

508 509 1056

522 523 1057

526 527 1058

591 592 1059

546 547 1060

496 497 1061

482 483 1062

530 531 1063

496 497 1064

496 497 1065

514 515 1066

482 483 1067

498 499 1068

512 513 1069

516 517 1070

581 582 1071

528 529 1072

478 479 1073

464 465 1074

512 513 1075

478 479 1076

478 479 1077

496 497 1078

464 465 1079

480 481 1080

480 481 1081

498 499 1082

563 564 1083

514 515 1084

500 501 1085

548 549 1086

514 515 1087

514 515 1088

532 533 1089

500 501 1090

516 517 1091

530 531 1092

534 535 1093

599 600 1094

520 521 1095

470 471 1096

456 457 1097

504 505 1098

470 471 1099

470 471 1100

488 489 1101

456 457 1102

472 473 1103

486 487 1104

490 491 1105

555 556 1106

496 497 1107

482 483 1108

530 531 1109

496 497 1110

496 497 1111

514 515 1112

482 483 1113

498 499 1114

512 513 1115

516 517 1116

581 582 1117

542 543 1118

492 493 1119

478 479 1120

526 527 1121

492 493 1122

492 493 1123

510 511 1124

478 479 1125

494 495 1126

508 509 1127

512 513 1128

577 578 1129

550 551 1130

500 501 1131

486 487 1132

534 535 1133

500 501 1134

500 501 1135

518 519 1136

486 487 1137

501 502 1138

516 517 1139

520 521 1140

585 586 1141

588 589 1142

538 539 1143

524 525 1144

572 573 1145

538 539 1146

538 539 1147

556 557 1148

524 525 1149

540 541 1150

554 555 1151

558 559 1152

623 624 1153

508 509 1154

458 459 1155

444 445 1156

492 493 1157

458 459 1158

458 459 1159

476 477 1160

444 445 1161

460 461 1162

474 475 1163

478 479 1164

543 544 1165

618 619 1166

568 569 1167

554 555 1168

602 603 1169

568 569 1170

568 569 1171

586 587 1172

554 555 1173

570 571 1174

584 585 1175

588 589 1176

653 654 1177

494 495 1178

444 445 1179

430 431 1180

478 479 1181

444 445 1182

444 445 1183

462 463 1184

430 431 1185

446 447 1186

460 461 1187

464 465 1188

529 530 1189

506 507 1190

456 457 1191

442 443 1192

490 491 1193

456 457 1194

456 457 1195

474 475 1196

442 443 1197

458 459 1198

472 473 1199

476 477 1200

541 542 1201

592 593 1202

542 543 1203

528 529 1204

576 577 1205

542 543 1206

543 543 1207

561 562 1208

528 529 1209

544 545 1210

558 559 1211

562 563 1212

628 629 1213

538 539 1214

488 489 1215

474 475 1216

522 523 1217

488 489 1218

488 489 1219

506 507 1220

474 475 1221

490 491 1222

504 505 1223

508 509 1224

573 574 1225

510 511 1226

558 559 1227

524 525 1228

524 525 1229

510 511 1230

526 527 1231

540 541 1232

544 545 1233

609 610 1234

548 549 1235

498 499 1236

484 485 1237

532 533 1238

498 499 1239

498 499 1240

516 517 1241

484 485 1242

500 501 1243

514 515 1244

518 519 1245

583 584 1246

534 535 1247

484 485 1248

470 471 1249

518 519 1250

484 485 1251

484 485 1252

502 503 1253

470 471 1254

486 487 1255

500 501 1256

504 505 1257

569 570 1258

536 537 1259

486 487 1260

472 473 1261

520 521 1262

486 487 1263

486 487 1264

504 505 1265

472 473 1266

488 489 1267

502 503 1268

506 507 1269

571 572 1270

558 559 1271

508 509 1272

494 495 1273

542 543 1274

508 509 1275

508 509 1276

526 527 1277

494 495 1278

510 511 1279

524 525 1280

528 529 1281

593 594 1282

506 507 1283

456 457 1284

442 443 1285

490 491 1286

456 457 1287

456 457 1288

474 475 1289

442 443 1290

457 458 1291

472 473 1292

476 477 1293

541 542 1294

572 573 1295

522 523 1296

508 509 1297

556 557 1298

522 523 1299

522 523 1300

540 541 1301

508 509 1302

524 525 1303

538 539 1304

542 543 1305

607 608 1306

576 577 1307

526 527 1308

512 513 1309

560 561 1310

526 527 1311

526 527 1312

544 545 1313

512 513 1314

528 529 1315

542 543 1316

546 547 1317

611 612 1318

576 577 1319

526 527 1320

512 513 1321

560 561 1322

526 527 1323

526 527 1324

544 545 1325

512 513 1326

528 529 1327

542 543 1328

546 547 1329

611 612 1330

576 577 1331

526 527 1332

512 513 1333

560 561 1334

526 527 1335

526 527 1336

544 545 1337

512 513 1338

528 529 1339

542 543 1340

546 547 1341

611 612 1342

492 493 1343

442 443 1344

428 429 1345

476 477 1346

442 443 1347

442 443 1348

460 461 1349

428 429 1350

444 445 1351

458 459 1352

462 463 1353

527 528 1354

522 523 1355

472 473 1356

458 459 1357

472 473 1358

472 473 1359

472 473 1360

490 491 1361

458 459 1362

474 475 1363

488 489 1364

492 493 1365

557 558 1366

504 505 1367

454 455 1368

440 441 1369

488 489 1370

454 455 1371

454 455 1372

472 473 1373

440 441 1374

456 457 1375

470 471 1376

474 475 1377

539 540 1378

606 607 1379

556 557 1380

542 543 1381

590 591 1382

556 557 1383

556 557 1384

574 575 1385

542 543 1386

558 559 1387

572 573 1388

576 577 1389

641 642 1390

566 567 1391

516 517 1392

502 503 1393

550 551 1394

516 517 1395

516 517 1396

534 535 1397

502 503 1398

518 519 1399

532 533 1400

536 537 1401

601 602 1402

556 557 1403

506 507 1404

492 493 1405

540 541 1406

506 507 1407

506 507 1408

524 525 1409

492 493 1410

508 509 1411

522 523 1412

526 527 1413

591 592 1414

532 533 1415

482 483 1416

468 469 1417

516 517 1418

482 483 1419

482 483 1420

500 501 1421

468 469 1422

484 485 1423

498 499 1424

502 503 1425

567 568 1426

518 519 1427

468 469 1428

454 455 1429

502 503 1430

468 469 1431

468 469 1432

486 487 1433

454 455 1434

470 471 1435

484 485 1436

488 489 1437

553 554 1438

582 583 1439

532 533 1440

518 519 1441

566 567 1442

532 533 1443

532 533 1444

550 551 1445

518 519 1446

534 535 1447

548 549 1448

552 553 1449

617 618 1450

520 521 1451

470 471 1452

456 457 1453

504 505 1454

470 471 1455

470 471 1456

488 489 1457

456 457 1458

472 473 1459

486 487 1460

490 491 1461

555 556 1462

582 583 1463

532 533 1464

518 519 1465

566 567 1466

532 533 1467

532 533 1468

550 551 1469

518 519 1470

534 535 1471

548 549 1472

552 553 1473

617 618 1474

568 569 1475

518 519 1476

504 505 1477

552 553 1478

518 519 1479

518 519 1480

536 537 1481

504 505 1482

520 521 1483

534 535 1484

538 539 1485

603 604 1486

538 539 1487

488 489 1488

474 475 1489

522 523 1490

488 489 1491

488 489 1492

506 507 1493

474 475 1494

490 491 1495

504 505 1496

508 509 1497

573 574 1498

504 505 1499

454 455 1500

440 441 1501

488 489 1502

454 455 1503

454 455 1504

472 473 1505

440 441 1506

456 457 1507

470 471 1508

474 475 1509

539 540 1510

528 529 1511

478 479 1512

464 465 1513

512 513 1514

478 479 1515

478 479 1516

496 497 1517

464 465 1518

479 480 1519

494 495 1520

498 499 1521

563 564 1522

628 629 1523

578 579 1524

564 565 1525

612 613 1526

578 579 1527

578 579 1528

596 597 1529

564 565 1530

580 581 1531

594 595 1532

598 599 1533

663 664 1534

607 608 1535

556 557 1536

542 543 1537

591 592 1538

556 557 1539

556 557 1540

575 576 1541

542 543 1542

558 559 1543

572 573 1544

576 577 1545

642 643 1546

506 507 1547

456 457 1548

442 443 1549

490 491 1550

456 457 1551

474 475 1552

474 475 1553

442 443 1554

457 458 1555

472 473 1556

476 477 1557

541 542 1558

552 553 1559

502 503 1560

488 489 1561

536 537 1562

502 503 1563

502 503 1564

520 521 1565

488 489 1566

504 505 1567

518 519 1568

522 523 1569

587 588 1570

572 573 1571

522 523 1572

508 509 1573

556 557 1574

522 523 1575

522 523 1576

540 541 1577

508 509 1578

524 525 1579

538 539 1580

542 543 1581

607 608 1582

607 608 1583

556 557 1584

542 543 1585

591 592 1586

556 557 1587

556 557 1588

575 576 1589

542 543 1590

558 559 1591

572 573 1592

576 577 1593

642 643 1594

552 553 1595

502 503 1596

488 489 1597

536 537 1598

502 503 1599

502 503 1600

520 521 1601

488 489 1602

504 505 1603

518 519 1604

522 523 1605

587 588 1606

552 553 1607

502 503 1608

488 489 1609

536 537 1610

502 503 1611

502 503 1612

520 521 1613

488 489 1614

504 505 1615

518 519 1616

522 523 1617

587 588 1618

580 581 1619

530 531 1620

516 517 1621

564 565 1622

530 531 1623

530 531 1624

548 549 1625

516 517 1626

532 533 1627

546 547 1628

550 551 1629

615 616 1630

552 553 1631

502 503 1632

488 489 1633

536 537 1634

502 503 1635

502 503 1636

520 521 1637

488 489 1638

504 505 1639

518 519 1640

522 523 1641

587 588 1642

570 571 1643

520 521 1644

506 507 1645

554 555 1646

520 521 1647

520 521 1648

538 539 1649

506 507 1650

522 523 1651

536 537 1652

540 541 1653

605 606 1654

570 571 1655

520 521 1656

506 507 1657

554 555 1658

520 521 1659

538 539 1660

538 539 1661

506 507 1662

522 523 1663

536 537 1664

540 541 1665

605 606 1666

588 589 1667

538 539 1668

524 525 1669

572 573 1670

538 539 1671

538 539 1672

556 557 1673

524 525 1674

540 541 1675

554 555 1676

558 559 1677

623 624 1678

544 545 1679

494 495 1680

480 481 1681

528 529 1682

494 495 1683

494 495 1684

512 513 1685

480 481 1686

496 497 1687

510 511 1688

514 515 1689

579 580 1690

566 567 1691

516 517 1692

502 503 1693

550 551 1694

516 517 1695

516 517 1696

534 535 1697

502 503 1698

518 519 1699

532 533 1700

536 537 1701

601 602 1702

574 575 1703

524 525 1704

510 511 1705

558 559 1706

524 525 1707

524 525 1708

542 543 1709

510 511 1710

526 527 1711

540 541 1712

544 545 1713

609 610 1714

612 613 1715

562 563 1716

548 549 1717

596 597 1718

562 563 1719

562 563 1720

580 581 1721

548 549 1722

564 565 1723

578 579 1724

582 583 1725

647 648 1726

532 533 1727

482 483 1728

468 469 1729

516 517 1730

482 483 1731

482 483 1732

500 501 1733

468 469 1734

484 485 1735

498 499 1736

502 503 1737

567 568 1738

642 643 1739

592 593 1740

578 579 1741

626 627 1742

592 593 1743

592 593 1744

610 611 1745

578 579 1746

594 595 1747

608 609 1748

612 613 1749

677 678 1750

518 519 1751

468 469 1752

454 455 1753

502 503 1754

468 469 1755

468 469 1756

486 487 1757

454 455 1758

470 471 1759

484 485 1760

488 489 1761

553 554 1762

530 531 1763

480 481 1764

466 467 1765

514 515 1766

480 481 1767

480 481 1768

498 499 1769

466 467 1770

482 483 1771

496 497 1772

500 501 1773

565 566 1774

617 618 1775

567 568 1776

552 523 1777

601 602 1778

567 568 1779

567 568 1780

585 586 1781

552 553 1782

568 569 1783

582 583 1784

586 587 1785

652 653 1786

562 563 1787

512 513 1788

498 499 1789

546 547 1790

512 513 1791

512 513 1792

530 531 1793

498 499 1794

514 515 1795

528 529 1796

532 533 1797

597 598 1798

597 598 1799

548 549 1800

534 535 1801

582 583 1802

548 549 1803

548 549 1804

566 567 1805

534 535 1806

550 551 1807

564 565 1808

568 569 1809

633 634 1810

572 573 1811

522 523 1812

508 509 1813

556 557 1814

522 523 1815

522 523 1816

540 541 1817

508 509 1818

524 525 1819

538 539 1820

542 543 1821

607 608 1822

558 559 1823

508 509 1824

494 495 1825

542 543 1826

508 509 1827

526 527 1828

526 527 1829

494 495 1830

510 511 1831

524 525 1832

528 529 1833

593 594 1834

560 561 1835

510 511 1836

496 497 1837

544 545 1838

510 511 1839

510 511 1840

528 529 1841

496 497 1842

512 513 1843

526 527 1844

530 531 1845

595 596 1846

582 583 1847

532 533 1848

518 519 1849

566 567 1850

532 533 1851

532 533 1852

550 551 1853

518 519 1854

534 535 1855

548 549 1856

552 553 1857

617 618 1858

530 531 1859

480 481 1860

466 467 1861

514 515 1862

480 481 1863

480 481 1864

498 499 1865

466 467 1866

482 483 1867

496 497 1868

500 501 1869

565 566 1870

596 597 1871

546 547 1872

532 533 1873

580 581 1874

546 547 1875

546 547 1876

564 565 1877

532 533 1878

548 549 1879

562 563 1880

566 567 1881

631 632 1882

600 601 1883

550 551 1884

536 537 1885

584 585 1886

550 551 1887

550 551 1888

568 569 1889

536 537 1890

552 553 1891

566 567 1892

570 571 1893

635 636 1894

600 601 1895

550 551 1896

536 537 1897

584 585 1898

550 551 1899

550 551 1900

568 569 1901

536 537 1902

552 553 1903

566 567 1904

570 571 1905

635 636 1906

600 601 1907

550 551 1908

536 537 1909

584 585 1910

550 551 1911

550 551 1912

568 569 1913

536 537 1914

552 553 1915

566 567 1916

570 571 1917

635 636 1918

516 517 1919

466 467 1920

452 453 1921

500 501 1922

466 467 1923

466 467 1924

484 485 1925

452 453 1926

468 469 1927

482 483 1928

486 487 1929

551 552 1930

546 547 1931

496 497 1932

482 483 1933

530 531 1934

496 497 1935

496 497 1936

514 515 1937

482 483 1938

498 499 1939

512 513 1940

516 517 1941

581 582 1942

498 499 1943

448 449 1944

434 435 1945

482 483 1946

448 449 1947

448 449 1948

466 467 1949

434 435 1950

449 450 1951

464 465 1952

468 469 1953

533 534 1954

600 601 1955

550 551 1956

536 537 1957

584 585 1958

550 551 1959

550 551 1960

568 569 1961

536 537 1962

552 553 1963

566 567 1964

570 571 1965

635 636 1966

560 561 1967

510 511 1968

496 497 1969

544 545 1970

510 511 1971

510 511 1972

528 529 1973

496 497 1974

512 513 1975

526 527 1976

530 531 1977

595 596 1978

550 551 1979

500 501 1980

486 487 1981

534 535 1982

500 501 1983

500 501 1984

518 519 1985

486 487 1986

501 502 1987

516 517 1988

520 521 1989

585 586 1990

526 527 1991

476 477 1992

462 463 1993

510 511 1994

476 477 1995

476 477 1996

494 495 1997

462 463 1998

477 478 1999

492 493 2000

496 497 2001

561 562 2002

512 513 2003

462 463 2004

448 449 2005

496 497 2006

462 463 2007

462 463 2008

480 481 2009

448 449 2010

464 465 2011

478 479 2012

482 483 2013

547 548 2014

576 577 2015

526 527 2016

512 513 2017

560 561 2018

526 527 2019

526 527 2020

544 545 2021

512 513 2022

528 529 2023

542 543 2024

546 547 2025

611 612 2026

514 515 2027

464 465 2028

450 451 2029

498 499 2030

464 465 2031

464 465 2032

482 483 2033

450 451 2034

465 466 2035

480 481 2036

484 485 2037

549 550 2038

576 577 2039

526 527 2040

512 513 2041

560 561 2042

526 527 2043

526 527 2044

544 545 2045

512 513 2046

528 529 2047

542 543 2048

546 547 2049

611 612 2050

562 563 2051

512 513 2052

498 499 2053

546 547 2054

512 513 2055

512 513 2056

530 531 2057

498 499 2058

514 515 2059

528 529 2060

532 533 2061

597 598 2062

532 533 2063

482 483 2064

468 469 2065

516 517 2066

482 483 2067

482 483 2068

500 501 2069

468 469 2070

484 485 2071

498 499 2072

502 503 2073

567 568 2074

498 499 2075

448 449 2076

434 435 2077

482 483 2078

448 449 2079

448 449 2080

466 467 2081

434 435 2082

449 450 2083

464 465 2084

468 469 2085

533 534 2086

522 523 2087

472 473 2088

458 459 2089

506 507 2090

472 473 2091

472 473 2092

490 491 2093

458 459 2094

473 474 2095

487 488 2096

492 493 2097

557 558 2098

622 623 2099

572 573 2100

558 559 2101

606 607 2102

572 573 2103

572 573 2104

590 591 2105

558 559 2106

574 575 2107

588 589 2108

592 593 2109

657 658 2110

600 601 2111

550 551 2112

536 537 2113

584 585 2114

550 551 2115

550 551 2116

569 570 2117

536 537 2118

552 553 2119

566 567 2120

570 571 2121

636 637 2122

500 501 2123

450 451 2124

436 437 2125

484 485 2126

450 451 2127

450 451 2128

468 469 2129

436 437 2130

451 452 2131

465 466 2132

470 471 2133

535 536 2134

546 547 2135

496 497 2136

482 483 2137

530 531 2138

496 497 2139

496 497 2140

514 515 2141

482 483 2142

498 499 2143

512 513 2144

516 517 2145

581 582 2146

566 567 2147

516 517 2148

502 503 2149

550 551 2150

516 517 2151

516 517 2152

534 535 2153

502 503 2154

518 519 2155

532 533 2156

536 537 2157

601 602 2158

600 601 2159

550 551 2160

536 537 2161

584 585 2162

550 551 2163

550 551 2164

569 570 2165

536 537 2166

552 553 2167

566 567 2168

570 571 2169

636 637 2170

546 547 2171

496 497 2172

482 483 2173

530 531 2174

496 497 2175

496 497 2176

514 515 2177

482 483 2178

498 499 2179

512 513 2180

516 517 2181

581 582 2182

546 547 2183

496 497 2184

482 483 2185

530 531 2186

496 497 2187

496 497 2188

514 515 2189

482 483 2190

498 499 2191

5112 513 2192

516 517 2193

581 582 2194

574 575 2195

524 525 2196

510 511 2197

558 559 2198

524 525 2199

524 525 2200

542 543 2201

510 511 2202

526 527 2203

540 541 2204

544 545 2205

609 610 2206

546 547 2207

496 497 2208

482 483 2209

530 531 2210

496 497 2211

496 497 2212

514 515 2213

482 483 2214

498 499 2215

512 513 2216

516 517 2217

581 582 2218

564 565 2219

514 515 2220

500 501 2221

548 549 2222

514 515 2223

514 515 2224

532 533 2225

500 501 2226

516 517 2227

530 531 2228

534 535 2229

599 600 2230

564 565 2231

514 515 2232

500 501 2233

548 549 2234

514 515 2235

514 515 2236

532 533 2237

500 501 2238

516 517 2239

530 531 2240

534 535 2241

599 600 2242

582 583 2243

532 533 2244

518 519 2245

566 567 2246

532 533 2247

532 533 2248

550 551 2249

518 519 2250

534 535 2251

548 549 2252

552 553 2253

617 618 2254

538 539 2255

488 489 2256

474 475 2257

522 523 2258

488 489 2259

488 489 2260

506 507 2261

474 475 2262

490 491 2263

504 505 2264

508 509 2265

573 574 2266

560 561 2267

510 511 2268

496 497 2269

544 545 2270

510 511 2271

510 511 2272

528 529 2273

496 497 2274

512 513 2275

526 527 2276

530 531 2277

595 596 2278

568 569 2279

518 519 2280

504 505 2281

552 553 2282

518 519 2283

518 519 2284

536 537 2285

504 505 2286

519 520 2287

534 535 2288

538 539 2289

603 604 2290

606 607 2291

556 557 2292

542 543 2293

590 591 2294

556 557 2295

556 557 2296

574 575 2297

542 543 2298

558 559 2299

572 573 2300

576 577 2301

641 642 2302

526 527 2303

476 477 2304

462 463 2305

510 511 2306

476 477 2307

476 477 2308

494 495 2309

462 463 2310

478 479 2311

492 493 2312

496 497 2313

561 562 2314

636 637 2315

586 587 2316

572 573 2317

620 621 2318

586 587 2319

586 587 2320

604 605 2321

572 573 2322

588 589 2323

602 603 2324

606 607 2325

671 672 2326

512 513 2327

462 463 2328

448 449 2329

496 497 2330

462 463 2331

462 463 2332

480 481 2333

448 449 2334

464 465 2335

478 479 2336

482 483 2337

547 548 2338

5244 525 2339

474 475 2340

460 461 2341

508 509 2342

474 475 2343

474 475 2344

492 493 2345

460 461 2346

476 477 2347

490 491 2348

494 495 2349

559 560 2350

610 611 2351

560 561 2352

546 547 2353

594 595 2354

560 561 2355

560 561 2356

579 580 2357

546 547 2358

562 563 2359

576 577 2360

580 581 2361

646 647 2362

556 557 2363

506 507 2364

492 493 2365

540 541 2366

506 507 2367

506 507 2368

524 525 2369

492 493 2370

508 509 2371

522 523 2372

526 527 2373

591 592 2374

592 593 2375

542 543 2376

528 529 2377

576 577 2378

542 543 2379

542 543 2380

560 561 2381

528 529 2382

544 545 2383

558 559 2384

562 563 2385

627 628 2386

566 567 2387

516 517 2388

502 503 2389

550 551 2390

516 517 2391

516 517 2392

534 535 2393

502 503 2394

518 519 2395

532 533 2396

536 537 2397

601 602 2398

552 553 2399

502 503 2400

488 489 2401

536 537 2402

502 503 2403

502 503 2404

520 521 2405

488 489 2406

504 505 2407

518 519 2408

522 523 2409

587 588 2410

554 555 2411

504 505 2412

490 491 2413

538 539 2414

504 505 2415

504 505 2416

522 523 2417

40 491 2418

506 507 2419

520 521 2420

524 525 2421

589 590 2422

550 551 2423

500 501 2424

486 487 2425

534 535 2426

500 501 2427

500 501 2428

518 519 2429

486 487 2430

502 503 2431

516 517 2432

520 521 2433

585 586 2434

524 525 2435

474 475 2436

460 461 2437

508 509 2438

474 475 2439

474 475 2440

492 493 2441

460 461 2442

475 476 2443

490 491 2444

494 495 2445

559 560 2446

590 591 2447

540 541 2448

526 527 2449

574 575 2450

540 541 2451

540 541 2452

558 559 2453

526 527 2454

542 543 2455

556 557 2456

560 561 2457

625 626 2458

594 595 2459

544 545 2460

530 531 2461

578 579 2462

544 545 2463

544 545 2464

562 563 2465

530 531 2466

546 547 2467

560 561 2468

564 565 2469

629 630 2470

594 595 2471

544 545 2472

530 531 2473

578 579 2474

544 545 2475

544 545 2476

562 563 2477

530 531 2478

546 547 2479

560 561 2480

564 565 2481

629 630 2482

594 595 2483

544 545 2484

530 531 2485

578 579 2486

544 545 2487

544 545 2488

562 563 2489

530 531 2490

546 547 2491

560 561 2492

564 565 2493

629 630 2494

510 511 2495

460 461 2496

446 447 2497

494 495 2498

460 461 2499

460 461 2500

478 479 2501

446 447 2502

461 462 2503

476 477 2504

480 481 2505

545 546 2506

540 541 2507

490 491 2508

476 477 2509

524 525 2510

490 491 2511

490 491 2512

508 509 2513

476 477 2514

492 493 2515

506 507 2516

510 511 2517

575 576 2518

510 511 2519

460 461 2520

446 447 2521

494 495 2522

460 461 2523

460 461 2524

478 479 2525

446 447 2526

462 463 2527

476 477 2528

480 481 2529

545 546 2530

612 613 2531

548 549 2532

548 549 2533

596 597 2534

562 563 2535

562 563 2536

580 581 2537

548 549 2538

564 565 2539

578 579 2540

582 583 2541

647 648 2542

572 573 2543

522 523 2544

508 509 2545

556 557 2546

522 523 2547

522 523 2548

540 541 2549

508 509 2550

524 525 2551

538 539 2552

542 543 2553

607 608 2554

562 563 2555

512 513 2556

498 499 2557

546 547 2558

512 513 2559

512 513 2560

530 531 2561

498 499 2562

514 515 2563

528 529 2564

532 533 2565

597 598 2566

538 539 2567

488 489 2568

474 475 2569

522 523 2570

488 489 2571

488 489 2572

506 507 2573

474 475 2574

490 491 2575

504 505 2576

508 509 2577

573 574 2578

524 525 2579

474 475 2580

460 461 2581

508 509 2582

474 475 2583

474 475 2584

492 493 2585

460 461 2586

476 477 2587

490 491 2588

494 495 2589

559 560 2590

588 589 2591

538 539 2592

524 525 2593

572 573 2594

538 539 2595

538 539 2596

556 557 2597

524 525 2598

540 541 2599

554 555 2600

558 559 2601

623 624 2602

526 527 2603

476 477 2604

462 463 2605

510 511 2606

476 477 2607

476 477 2608

494 495 2609

462 463 2610

478 479 2611

492 493 2612

496 497 2613

561 562 2614

588 589 2615

538 539 2616

524 525 2617

572 573 2618

538 539 2619

538 539 2620

556 557 2621

524 525 2622

540 541 2623

554 555 2624

558 559 2625

623 624 2626

574 575 2627

524 525 2628

510 511 2629

558 559 2630

524 525 2631

524 525 2632

542 543 2633

510 511 2634

526 527 2635

540 541 2636

544 545 2637

609 610 2638

544 545 2639

494 495 2640

480 481 2641

494 495 2642

494 495 2643

494 495 2644

512 513 2645

480 481 2646

496 497 2647

510 511 2648

514 515 2649

579 580 2650

510 511 2651

460 461 2652

446 447 2653

494 495 2654

460 461 2655

460 461 2656

478 479 2657

446 447 2658

462 463 2659

476 477 2660

480 481 2661

545 546 2662

534 535 2663

484 485 2664

470 471 2665

518 518 2666

484 485 2667

484 485 2668

502 503 2669

470 471 2670

486 487 2671

500 501 2672

504 505 2673

569 570 2674

634 635 2675

584 585 2676

570 571 2677

618 619 2678

584 585 2679

584 585 2680

602 603 2681

570 571 2682

586 587 2683

600 601 2684

604 605 2685

669 670 2686

613 614 2687

563 564 2688

548 549 2689

597 598 2690

563 564 2691

563 564 2692

581 582 2693

548 549 2694

564 565 2695

578 579 2696

582 583 2697

648 649 2698

512 513 2699

462 463 2700

448 449 2701

496 497 2702

462 463 2703

462 463 2704

480 481 2705

448 449 2706

463 464 2707

478 479 2708

482 483 2709

547 548 2710

558 559 2711

508 509 2712

494 495 2713

542 543 2714

508 509 2715

508 509 2716

526 527 2717

494 495 2718

510 511 2719

524 525 2720

528 529 2721

593 594 2722

578 579 2723

528 529 2724

514 515 2725

562 563 2726

528 529 2727

528 529 2728

546 547 2729

514 515 2730

530 531 2731

544 545 2732

548 549 2733

613 614 2734

613 614 2735

563 564 2736

548 549 2737

597 598 2738

563 564 2739

563 564 2740

581 582 2741

548 549 2742

564 565 2743

578 579 2744

582 583 2745

648 649 2746

558 559 2747

508 509 2748

494 495 2749

542 543 2750

508 509 2751

508 509 2752

526 527 2753

494 495 2754

510 511 2755

524 525 2756

528 529 2757

593 594 2758

558 559 2759

508 509 2760

494 495 2761

542 543 2762

508 509 2763

508 509 2764

526 527 2765

494 495 2766

510 511 2767

524 525 2768

528 529 2769

593 594 2770

586 587 2771

536 537 2772

522 523 2773

570 571 2774

536 537 2775

536 537 2776

554 555 2777

522 523 2778

538 539 2779

552 553 2780

556 557 2781

621 622 2782

558 559 2783

508 509 2784

494 495 2785

542 543 2786

508 509 2787

508 509 2788

526 527 2789

494 495 2790

510 511 2791

524 525 2792

528 529 2793

593 594 2794

576 577 2795

526 527 2796

512 513 2797

560 561 2798

526 527 2799

526 527 2800

544 545 2801

512 513 2802

528 529 2803

542 543 2804

546 547 2805

611 612 2806

576 577 2807

526 527 2808

512 513 2809

560 561 2810

526 527 2811

526 527 2812

544 545 2813

512 513 2814

542 543 2815

542 543 2816

546 547 2817

611 612 2818

594 595 2819

544 545 2820

530 531 2821

578 579 2822

544 545 2823

544 545 2824

562 563 2825

530 531 2826

546 547 2827

560 561 2828

564 565 2829

629 630 2830

550 551 2831

500 501 2832

486 487 2833

534 535 2834

500 501 2835

500 501 2836

518 519 2837

486 487 2838

502 503 2839

516 517 2840

520 521 2841

585 586 2842

572 573 2843

522 523 2844

508 509 2845

556 557 2846

522 523 2847

522 523 2848

540 541 2849

508 509 2850

524 525 2851

538 539 2852

542 543 2853

607 608 2854

580 581 2855

530 531 2856

516 517 2857

564 565 2858

530 531 2859

530 531 2860

548 5549 2861

516 517 2862

532 533 2863

546 547 2864

550 551 2865

615 616 2866

618 619 2867

568 569 2868

554 555 2869

602 603 2870

568 569 2871

568 569 2872

586 587 2873

554 555 2874

570 571 2875

584 585 2876

588 589 2877

653 654 2878

538 539 2879

488 489 2880

474 475 2881

522 523 2882

488 489 2883

488 489 2884

506 507 2885

474 475 2886

490 491 2887

504 505 2888

508 509 2889

573 574 2890

648 649 2891

598 599 2892

584 585 2893

632 633 2894

598 599 2895

598 599 2896

616 617 2897

584 585 2898

600 601 2899

614 615 2900

618 619 2901

683 684 2902

622 623 2903

585 586 2904

619 620 2905

619 620 2906

585 586 2907

568 569 2908

583 584 2909

568 569 2910

462 463 2911

589 590 2912

589 590 2913

639 640 2914

571 572 2915

577 578 2916

617 618 2917

617 618 2918

583 584 2919

617 618 2920

617 618 2921

617 618 2922

599 600 2923

599 600 2924

639 640 2925

591 592 2926

591 592 2927

564 565 2928

554 555 2929

597 598 2930

659 660 2931

599 600 2932

599 600 2933

689 690 2934

569 570 2935

569 570 2936

571 572 2937

571 572 2938

633 634 2939

564 565 2940

571 572 2941

605 606 2942

608 609 2943

580 581 2944

605 606 2945

741 742 2946

550 501 2947

659 660 2948

625 626 2949

659 660 2950

554 555 2951

648 649 2952

659 660 2953

659 660 2954

659 660 2955

592 593 2956

667 668 2957

667 668 2958

565 566 2959

592 593 2960

592 593 2961

599 600 2962

667 668 2963

702 703 2964

688 689 2965

667 668 2966

512 513 2967

536 537 2968

659 660 2969

592 593 2970

592 593 2971

592 593 2972

617 618 2973

615 616 2974

588 589 2975

691 692 2976

566 567 2977

589 590 2978

571 572 2979

501 502 2980

599 600 2981

623 624 2982

552 553 2983

641 642 2984

579 580 2985

593 594 2986

613 614 2987

627 628 2988

605 606 2989

619 620 2990

625 626 2991

591 592 2992

617 618 2993

643 644 2994

667 668 2995

669 670 2996

555 556 2997

639 640 2998

637 638 2999

596 597 3000

581 582 3001

579 580 3002

625 626 3003

623 624 3004

659 660 3005

657 658 3006

595 596 3007

597 598 3008

669 670 3009

576 577 3010

574 575 3011

590 591 3012

611 612 3013

609 610 3014

611 612 3015

627 628 3016

639 640 3017

597 598 3018

623 624 3019

609 610 3020

681 682 3021

679 680 3022

578 579 3023

605 606 3024

611 612 3025

603 604 3026

605 606 3027

589 590 3028

808 809 3029

575 576 3030

605 606 3031

741 742 3032

618 619 3033

742 743 3034

539 540 3035

565 566 3036

565 566 3037

624 625 3038

541 542 3039

73 735 3040

575 576 3041

617 618 3042

566 567 3043

550 551 3044

647 648 3045

690 691 3046

555 556 3047

636 637 3048

664 665 3049

594 595 3050

655 656 3051

653 654 3052

578 579 3053

590 591 3054

577 578 3055

617 618 3056

576 577 3057

645 646 3058

609 610 3059

526 527 3060

528 529 3061

512 513 3062

542 543 3063

592 593 3064

597 598 3065

554 555 3066

554 555 3067

554 555 3068

639 640 3069

576 577 3070

598 599 3071

590 591 3072

590 591 3073

639 640 3074

639 640 3075

639 640 3076

583 584 3077

590 591 3078

579 580 3079

564 565 3080

569 570 3081

667 668 3082

564 565 3083

613 614 3084

721 722 3085

613 614 3086

579 580 3087

660 661 3088

568 569 3089

628 629 3090

584 585 3091

598 599 3092

667 668 3093

582 583 3094

624 625 3095

609 610 3096

570 571 3097

694 695 3098

694 695 3099

694 695 3100

694 695 3101

694 695 3102

694 695 3103

639 640 3104

615 616 3105

631 632 3106

680 681 3107

682 683 3108

637 638 3109

673 674 3110

689 690 3111

631 632 3112

615 616 3113

669 670 3114

640 641 3115

696 697 3116

611 612 3117

725 726 3118

612 613 3119

708 709 3120

615 616 3121

464 465 3122

478 479 3123

572 573 3124

572 573 3125

490 491 3126

504 505 3127

437 438 3128

541 542 3129

571 572 3130

599 600 3131

569 570 3132

567 568 3133

468 469 3134

453 454 3135

616 617 3136

574 575 3137

590 591 3138

688 689

TABLE 2C The [4, 4, 0] REVERSE TURN MIMETICS LIBRARY M + H No. MOLSTRUCTURE M.W (MASS) 1

615.68 C31H30FN7O4S 616.68 2

658.70 C33H31FN6O6S 659.70 3

689.76 C37H32FN7O4S 690.76 4

630.76 C23H31FN6O3S2 631.76 5

630.73 C33H35FN6O4S 631.73 6

632.66 C31H29FN6O6S 633.66 7

688.77 C38H33FN6O4S 689.77 8

628.72 C33H33FN6O4S 629.72 9

615.68 C31H30FN7O4S 616.68 10

615.68 C31H30FN7O4S 616.68 11

579.65 C32H33N7O4 580.65 12

713.78 C40H39N7O6 714.78 13

683.80 C40H41N7O4 684.80 14

561.62 C31H33F2N5O3 562.62 15

714.77 C39H38N8O6 715.77 16

684.79 C39H40N8O4 685.79 17

620.72 C30H29FN6O4S2 621.72 18

790.97 C43H50N8O5S 791.97 19

683.58 C32H29Cl2FN6O4S 684.58 20

620.74 C32H37FN6O4S 621.74 21

628.72 C33H33FN6O4S 629.72 22

650.67 C32H29F3N6O4S 651.67 23

610.73 C33H34N6O4S 611.73 24

634.75 C31H31FN6O4S2 635.75 25

573.64 C30H28FN5O4S 574.64 26

628.72 C33H33FN6O4S 629.72 27

615.68 C31H30FN7O4S 616.68 28

674.74 C34H35FN6O6S 675.74 29

639.70 C33H30FN7O4S 640.70 30

670.78 C35H38N6O6S 671.78 31

735.66 C32H32N7Na2O7PS 736.66 32

632.68 C32H30F2N6O4S 633.68 33

683.58 C32H29Cl2FN6O4S 684.58 34

629.70 C34H39N5O7 630.70 35

599.68 C33H37N5O6 600.68 36

674.74 C34H35FN6O6S 675.74 37

638.71 C34H31FN6O4S 639.71 38

723.62 C33H36N5Na2O9P 724.62 39

782.64 C33H30FN6Na2O9PS 783.64 40

703.59 C32H32N7Na2O7P 704.59 41

792.73 C37H43N6Na2O9P 793.73 42

746.66 C35H37N6Na2O8P 747.66 43

732.85 C40H40N6O6S 733.85 44

578.66 C33H34N6O4 579.66 45

579.65 C32H33N7O4 580.65 46

587.64 C32H34FN5O5 588.64 47

611.73 C35H41N5O5 612.73 48

593.68 C33H35N7O4 594.68 49

604.10 C32H34ClN5O5 605.10 50

587.64 C32H34FN5O5 588.64 51

595.69 C34H37N5O5 596.69 52

593.68 C33H35N7O4 594.68 53

619.51 C30H31BrN6O4 620.51 54

648.55 C32H34BrN5O5 649.55 55

782.69 C37H37N8Na2O7P 783.69 56

574.62 C31H32F2N6O3 575.62 57

595.73 C35H41N5O4 596.73 58

686.77 C37H43FN6O6 687.77 59

583.68 C33H37N5O5 584.68 60

625.76 C36H43N5O5 626.76 61

597.70 C34H39N5O5 598.70 62

703.59 C32H32N7Na2O7P 704.59 63

553.65 C32H35N5O4 554.65 64

590.62 C31H32F2N6O4 591.62 65

719.63 C34H36N5Na2O8P 720.63 66

774.88 C43H42N6O7S 775.88 67

620.70 C35H36N6O5 621.70 68

595.69 C34H37N5O5 596.69 69

608.73 C35H40N6O4 609.73 70

565.66 C33H35N5O4 566.66 71

654.68 C31H32F2N6O6S 655.68 72

711.58 C32H33FN5Na2O8P 712.58 73

628.63 C32H32N6O8 629.63 74

732.67 C35H39N6Na2O7P 733.67 75

728.04 C32H33ClN5Na2O8P 729.04 76

856.79 C40H39N6Na2O9PS 857.79 77

717.62 C33H34N7Na2O7P 718.62 78

633.74 C36H39N7O4 634.74 79

619.11 C32H35ClN6O5 620.11 80

619.62 C32H31F2N5O6 620.62 81

600.66 C32H36N6O6 601.66 82

580.64 C31H32N8O4 581.64 83

733.84 C39H39N7O6S 734.84 84

579.65 C32H33N7O4 580.65 85

605.63 C32H33F2N5O5 606.63 86

800 C44H44N6O7S 801.92 87

753.27 C39H37ClN6O6S 754.27 88

603.62 C32H31F2N5O5 604.62 89

533.69 534.69 90

646.73 C37H38N6O5 647.73 91

487.55 C27H29N5O4 488.55 92

597.66 C33H35N5O6 598.66 93

583.63 C32H33N5O6 584.63 94

732.73 C37H38F2N6O8 733.73 95

757.68 C36H38N7Na2O7P 758.68 96

743.56 C32H30F2N5Na2O9P 744.56 97

732.67 C35H39N6Na2O7P 733.67 98

724.61 C32H35N6Na2O9P 725.61 99

668.71 C32H34F2N6O6S 669.71 100

595.71 C33H33N5O4S 596.71 101

712.75 C37H40N6O9 713.75 102

657.76 C38H39N7O4 658.76 103

759.64 C36H38IN7O4 760.64 105

646.73 C37H38N6O5 647.73 106

716.85 C40H40N6O5S 717.85 107

756.87 C42H40N6O6S 757.87 108

858.74 C40H39IN6O6S 859.74 109

795.30 C41H39ClN6O7S 796.30 110

585.72 C32H35N5O4S 586.72 111

629.70 C37H35N5O5 630.70 112

623.70 C35H37N5O6 624.70 113

725.57 C33H36IN5O6 726.57 114

658.73 C32H34N8O6S 659.73 115

598.69 C34H38N4O6 599.69 116

593.68 C33H35N7O4 594.68 117

898.83 C42H41N6Na2O10PS 899.83 118

744.64 C35H35N6Na2O8P 745.64 119

919.25 C41H38ClN6Na2O10PS 920.25 120

877.21 C39H36ClN6Na2O9PS 878.21 121

857.78 C39H38N7Na2O9PS 858.78 122

617.72 C32H35N5O6S 618.72 123

579.65 C32H33N7O4 580.65 124

722.63 C34H37N4Na2O9P 723.63 125

632.71 C36H36N6O5 633.71 126

378.76 C33H38N6O8S 679.76 127

592.69 C34H36N6O4 593.69 128

682.23 C37H36ClN5O4S 683.23 129

732.85 C40H40N6O6S 733.85 130

714.23 C37H36ClN5O6S 715.23 131

760.26 C38H38ClN5O8S 761.26 132

595.69 C34H37N5O5 596.69 133

625.76 C36H43N5O5 626.76 134

692.85 C39H48N8O4 693.85 135

719.65 C33H32N5Na2O7PS 720.65 136

709.66 C32H34N5Na2O7PS 710.66 137

625.71 C35H39N5O6 626.71 138

631.72 C37H37N5O5 632.72 139

658.79 C39H42N6O4 659.79 140

814.95 C34H35N6O7S 816.95 141

577.68 C33H35N7O3 578.68 142

660.76 C38H40N6O5 661.76 143

692.80 C39H44N6O6 693.80 144

762.87 C41H42N6O7S 763.87 145

788.01 C43H57N5O7S 789.01 146

623.74 C35H41N7O4 624.74 147

681.86 C40H41N5O5 682.86 148

767.29 C40H39ClN6O6S 768.29 149

770.68 C37H37N6Na2O8P 771.68 150

749.70 C36H42N5Na2O8P 750.70 151

703.59 C32H32N7Na2O7P 704.59 152

651.79 C38H45N5O5 652.79 153

613.11 C33H33ClN6O4 614.11 154

651.84 C39H49N5O4 652.84 155

696.84 C39H48N6O6 697.84 156

608.69 C34H36N6O5 609.69 157

652.74 C36H40N6O6 653.74 158

650.77 C37H42N6O5 651.77 159

761.93 C40H51N5O8S 762.93 160

639.74 C36H41N5O6 640.74 161

653.77 C37H43N5O6 654.77 162

679.74 C38H38FN5O6 680.74 163

701.81 C41H43N5O6 702.81 164

664.79 C38H44N6O5 665.79 165

666.77 C37H42N6O6 667.77 166

594.66 C32H34N8O4 595.66 167

595.68 C32H36N8O4 597.68 168

595.65 C32H33N7O5 596.65 169

618.63 C32H32F2N6O5 619.63 170

665.74 C36H39N7O6 666.74 171

584.62 C31H32N6O6 585.62 172

582.62 C32H31FN6O4 583.62 173

554.64 C31H34N6O4 555.64 174

623.70 C34H37N7O5 624.70 175

614.09 C32H32ClN7O4 615.09 176

853.96 C42H43N7O9S2 854.96 177

699.78 C35H37N7O7S 700.78 178

678.58 C31H33N6Na2O7P 679.58 179

738.04 C32H31ClN7O7P 739.04 180

683.75 C40H37N5O6 684.75 181

607.66 C34H33N5O6 608.66 182

745.87 C45H43N7O4 746.87 183

616.71 C36H36N6O4 617.71 184

655.75 C38H37N7O4 656.75 185

655.75 C38H37N7O4 656.75 186

725.81 C37H39N7O7S 726.81 187

701.79 C35H39N7O7S 702.79 188

814.91 C40H46N8O9S 815.91 189

840.95 C42H48N8O9S 841.95 190

674.79 C33H34N6O6S2 675.79 191

627.71 C33H33N5O6S 628.71 192

619.51 C30H31BrN6O4 620.51 193

616.71 C36H36N6O4 617.71 194

646.74 C37H38N6O5 647.74 195

694.80 C37H38N6O6S 695.80 196

634.70 C36H35FN6O4 635.70 197

646.74 C37H38N6O5 647.74 198

662.80 C37H38N6O4S 663.80 199

794.92 C45H42N6O6S 795.92 200

632.71 C36H36N6O5 633.71 201

641.72 C37H35N7O4 642.72 202

669.77 C39H39N7O4 670.77 203

618.52 C31H32BrN5O4 619.52 204

654.76 C39H38N6O4 655.76 205

580.68 C33H36N6O4 581.68 206

617.70 C35H35N7O4 618.70 207

918.86 C45H41N6Na2O9PS 919.86 208

778.70 C39H37N6Na2O7P 779.70 209

646.74 C37H38N6O5 647.74 210

580.68 C33H36N6O4 581.68 211

632.71 C36H36N6O5 633.71 212

646.74 C37H38N6O5 647.74 213

603.67 C34H33N7O4 604.67 214

743.83 C40H37N7O6S 744.83 215

617.70 C35H35N7O4 618.70 216

614.09 C32H32ClN7O4 615.09 217

616.71 C36H36N6O4 617.71 218

641.72 C37H35N7O4 642.72 219

646.74 C37H38N6O5 647.74 220

616.71 C36H36N6O4 617.71 221

620.74 C36H40N6O4 621.74 222

620.74 C36H40N6O4 621.74 223

664.75 C37H40N6O6 665.75 224

617.70 C35H35N7O4 618.70 225

556.62 C29H32N8O4 557.62 226

621.75 C35H35N5O4S 622.75 227

616.71 C36H36N6O4 617.71 228

647.72 C36H37N7O5 648.72 229

615.72 C37H37N5O4 616.72 230

579.65 C32H33N7O4 580.65 231

672.75 C39H37FN6O4 673.75 232

869.81 C45H42N7Na2O7P 870.81 233

640.73 C38H36N6O4 641.73 234

645.75 C38H39N5O5 646.75 235

753.65 C37H34N5Na2O8P 754 236

645.75 C38H39N5O5 646.75 237

581.66 C33H35N5O5 582.66 238

634.70 C36H35FN6O4 635.70 239

826.93 C46H43FN6O6S 827.93 240

687.81 C35H41N7O6S 688.81 241

631.72 C37H37N5O5 632.72 242

659.73 C38H37N5O6 660.73 243

582.65 C32H34N6O5 583.65 244

645.75 C38H39N5O5 646.75 245

646.74 C37H38N6O5 647.74 246

672.77 C39H40N6O5 673.77 247

676.74 C33H36N6O8 677.74 248

631.72 C36H37N7O4 632.72 249

701.81 C40H43N7O5 702.81 250

658.75 C38H38N6O5 659.75 251

630.74 C37H38N6O4 631.74 252

772.91 C43H44N6O6S 773.91 253

662.71 C32H34N6O8S 663.71 254

612.68 C33H36N6O6 613.68 255

583.64 C31H33N7O5 584.64 256

612.68 C33H36N6O6 613.68 257

598.65 C32H34N6O6 599.65 258

598.65 C32H34N6O6 599.65 259

626.70 C34H38N6O6 627.70 260

564.63 C32H32N6O4 565.63 261

584.62 C31H32N6O6 585.62 262

583.64 C31H33N7O5 584.64 263

651.15 C36H35ClN6O4 652.15 264

646.74 C37H38N6O5 647.74 265

579.65 C32H33N7O4 580.65 266

732.85 C40H40N6O6S 733.85 267

578.66 C33H34N6O4 579.66 268

582.62 C32H31FN6O4 583.62 269

607.66 C32H33N9O4 608.66 270

646.74 C37H38N6O5 647.74 271

636.51 C31H31BrFN5O4 637.51 272

646.74 C37H38N6O5 647.74 273

595.65 C32H33N7O5 596.65 274

697.78 C37H43N7O7 698.78 275

597.66 C32H35N7O5 598.66 276

634.70 C36H35FN6O4 635.70 277

650.77 C37H42N6O5 651.77 278

636.74 C36H40N6O5 637.74 279

736.82 C39H44N8O7 737.82 280

634.70 C36H35FN6O4 635.70 281

607.66 C32H33N9O4 608.66 282

634.70 C36H35FN6O4 635.70 283

678.80 C37H38N6O5S 679.80 284

672.77 C39H40N6O5 673.77 285

636.70 C34H36N8O5 637.70 286

632.71 C36H36N6O5 633.71 287

609.68 C33H35N7O5 610.68 288

673.76 C38H39N7O5 674.76 289

679.79 C36H37N7O5S 680.79 290

596.68 C33H36N6O5 597.68 291

634.72 C36H38N6O5 635.72 292

610.70 C34H38N6O5 611.70 293

594.66 C32H34N8O4 595.66 294

642.66 C33H34N6O8 643.66 295

611.69 C33H37N7O5 612.69 296

617.14 C33H37ClN6O4 618.14 297

594.66 C32H34N8O4 595.66 298

594.66 C32H34N8O4 595.66 299

636.74 C36H40N6O5 637.74 300

661.73 C32H35N7O7S 662.73 301

636.70 C34H36N8O5 637.70 302

627.65 C32H33N7O7 628.65 304

696.84 C39H48N6O6 670.84 305

605.69 C34H35N7O4 606.69 306

690.83 C40H46N6O5 691.83 307

624.73 C35H40N6O5 625.73 308

640.73 C35H40N6O6 641.73 309

678.82 C39H46N6O5 679.82 310

636.74 C36H40N6O5 637.74 311

648.71 C35H36N8O5 649.71 312

633.63 C32H36N5O7P 634.63 313

539.63 C31H33N5O4 540.63 314

563.65 C33H33N5O4 564.65 315

567.73 568.73 316

522.62 523.62 317

504.60 505.60 318

531.67 532.67 319

588.75 589.75 320

585.72 586.72 321

536.72 537.72 322

572.72 573.72 323

656.19 657.19 324

562.68 563.68 325

636.23 637.23 326

686.87 687.87 327

557.66 558.66 328

601.68 602.68 329

679.27 680.27 330

566.74 567.74 331

571.73 572.73 332

539.65 540.65 333

524.59 525.59 334

569.68 570.68 335

598.72 599.72 336

460.53 461.53 337

525.67 526.67 338

421.54 422.54 339

518.61 519.61 340

445.56 446.56 341

536.63 537.63 342

500.60 501.60 343

517.62 518.62 344

540.68 541.68 345

486.61 487.61 346

489.53 490.53 347

523.63 524.63 348

551.64 552.64 349

534.65 535.65 350

620.78 621.78 351

612.16 613.16 352

540.70 541.70 353

536.63 537.63 354

565.71 566.71 In addition, synthesis of the peptide mimetics of the library of the present invention may be accomplished using the General Scheme of [4,3,0] Reverse-Turn Mimetic Library as follows:

Synthesis of the peptide mimetics of the bicyclic template libraries of the present invention was accomplished using FlexChem Reactor Block which has 96 well plate by known techniques. In the above scheme ‘Pol’ represents Bromoacetal resin (Advanced ChemTech) and detailed procedure is illustrated below.

Step 1

The bromoacetal resin (1.6 mmol/g) and a solution of R1 amine in DMSO (2M solution) were placed in 96 well Robbins block (FlexChem). The reaction mixture was shaken at 60° C. using rotating oven [Robbins Scientific] for 12 hours. The resin was washed with DMF, MeOH, and then DCM

Step 2

A solution of commercial available Fmoc-Amino Acids (4 equiv.), PyBob (4 equiv.), HOAt (4 equiv.), and DIEA (12 equiv.) in DMF was added to the resin. After the reaction mixture was shaken for 12 hours at room temperature, the resin was washed with DMF, MeOH, and then DCM.

Step 3

To the resin swollen by DMF before reaction was added 25% piperidine in DMF. After the reaction mixture was shaken for 30 min at room temperature. This deprotection step was repeated again and then washed with DMF, Methanol, then DCM. A solution of hydrazine carbamoyl chloride (4 equiv.), HOBt (4 equiv.), and DIC (4 equiv.) in DMF was added to the resin. After the reaction mixture was shaken for 12 hours at room temperature, the resin was washed with DMF, MeOH, and then DCM.

Step 4

To the resin swollen by DMF before reaction was added 25% piperidine in DMF. After the reaction mixture was shaken for 30 min at room temperature. This deprotection step was repeated again and then washed with DMF, Methanol, then DCM. To the resin swollen by DCM before reaction was added R₁-isocynate (5 equiv.) in DCM. After the reaction mixture was shaken for 12 hours at room temperature the resin was washed with DMF, MeOH, then DCM.

Step 5

The resin was treated with formic acid (1.2 mL each well) for 18 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under reduced pressure using Speed Vac [SAVANT] to give the product as oil. These products were diluted with 50% water/acetonitrile and then lyophilized after freezing.

Table 3 shows a [4,3,0] reverse turn mimetics library which can be prepared according to the present invention, of which representative preparation is given in Example 5.

TABLE 3 THE [4,3,0] REVERSE TURN MIMETRICS LIBRARY

Mol. No R₂ R₄ R₆ R₁ Weight M + H 610 Isoamyl 4-HO-phenyl Methyl Phenyl 466 467 611 Isoamyl 4-HO-phenyl Methyl 4-Me-phenyl 480 481 612 Isoamyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 494 495 613 Isoamyl 4-HO-phenyl Methyl 4-MeO-phenyl 496 497 614 Isoamyl 4-HO-phenyl Methyl 4-CF₃-phenyl 534 535 615 Isoamyl 4-HO-phenyl Methyl Cyolohexyl 472 473 616 Isoamyl 4-HO-phenyl Methyl Benzyl 480 481 617 Isoamyl 4-HO-phenyl Methyl

494 495 618 Isoamyl 4-HO-phenyl Methyl 4-MeO-benzyl 510 511 619 Isoamyl 4-HO-phenyl Methyl Phenethyl 494 495 620 Isoamyl 4-HO-phenyl Methyl Pentyl 460 461 621 Isoamyl 4-HO-phenyl Methyl Hexyl 474 475 622 Benzyl 4-HO-phenyl Methyl Phenyl 486 487 623 Benzyl 4-HO-phenyl Methyl 4-Me-phenyl 500 501 624 Benzyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 514 515 625 Benzyl 4-HO-phenyl Methyl 4-MeO-phenyl 516 517 626 Benzyl 4-HO-phenyl Methyl 4-CF₃-phenyl 554 555 627 Benzyl 4-HO-phenyl Methyl Cyclohexyl 492 493 628 Benzyl 4-HO-phenyl Methyl Benzyl 500 501 629 Benzyl 4-HO-phenyl Methyl

514 515 630 Benzyl 4-HO-phenyl Methyl 4- MeO-benzyl 530 531 631 Benzyl 4-HO-phenyl Methyl Phenethyl 514 515 632 Benzyl 4-HO-phenyl Methyl Pentyl 480 481 633 Benzyl 4-HO-phenyl Methyl Hexyl 494 495 634 Naphth-1-ylmethyl 4-HO-phenyl Methyl Phenyl 536 537 635 Naphth-1-ylmethyl 4-HO-phenyl Methyl 4-Me-phenyl 550 551 636 Naphth-1-ylmethyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 564 565 637 Naphth-1-ylmethyl 4-HO-phenyl Methyl 4-MeO-phenyl 566 567 638 Naphth-1-ylmethyl 4-HO-phenyl Methyl 4-CF₃-phenyl 604 605 639 Naphth-1-ylmethyl 4-HO-phenyl Methyl Cyclohexyl 542 643 640 Naphth-1-methyl 4-HO-phenyl Methyl Benzyl 550 551 641 Naphth-1-ylmethl 4-HO-phenyl Methyl

564 565 642 Naphth-1-ylmethyl 4-HO-phenyl Methyl 4-MeO-benzyl 580 581 643 Naphth-1-ylmethyl 4-HO-phenyl Methyl Phenethyl 564 565 644 Nephth-1-ylmethyl 4-HO-phenyl Methyl Pentyl 530 531 645 Naphth-1-ylmethyl 4-HO-phenyl Methyl Hexyl 544 545 646 Cyolohexylmethyl 4-HO-phenyl Methyl Phenyl 492 493 647 Cyolohexylmethyl 4-HO-phenyl Methyl 4-Me-phenyl 506 507 648 Cyolohexylmethyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 520 521 649 Cyclohoxylmethyl 4-HO-phenyl Methyl 4-MeO-phenyl 522 523 650 Cyolohexylmethyl 4-HO-phenyl Methyl 4-CF₃-phenyl 560 561 651 Cyolohexylmethyl 4-HO-phenyl Methyl Cyclohexyl 468 469 652 Cyolohexylmethyl 4-HO-phenyl Methyl Benzyl 506 507 653 Cyolohexylmethyl 4-HO-phenyl Methyl

520 521 654 Cyclohexylmethyl 4-HO-phenyl Methyl 4-MeO-benzyl 536 537 655 Cyolohexylmethyl 4-HO-phenyl Methyl Phenethyl 520 521 656 Cyclohexylmethyl 4-HO-phenyl Methyl Pentyl 486 487 657 Cyolohexylmethyl 4-HO-phenyl Methyl Hexyl 500 501 658 4-methylbenzyl 4-HO-phenyl Methyl Phenyl 500 501 659 4-methylbenzyl 4-HO-phenyl Methyl 4-Me-phenyl 514 515 660 4-methylbenzyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 528 529 661 4-methylbenzyl 4-HO-phenyl Methy 4-MeO-phenyl 530 531 662 4-methylbenzyl 4-HO-phenyl Methyl 4-CF₃-phenyl 568 569 663 4-methylbenzyl 4-HO-phenyl Methyl Cyclohexyl 506 507 664 4-methylbenzyl 4-HO-phenyl Methyl Benzyl 514 515 665 4-methylbenzyl 4-HO-phenyl Methyl

523 529 666 4-methylbenzyl 4-HO-phenyl Methyl 4-MeO-benzyl 544 545 667 4-methylbenzyl 4-HO-phenyl Methyl Phenethyl 528 529 668 4-methylbenzyl 4-HO-phenyl Methyl Pentyl 494 495 669 4-methylbenzyl 4-HO-phenyl Methyl Hexyl 508 509 670 Methoxypropyl 4-HO-phenyl Methyl Phenyl 468 469 671 Methoxypropyl 4-HO-phenyl Methyl 4-Me-phenyl 482 483 672 Methoxypropyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 496 497 673 Methoxypropyl 4-HO-phenyl Methyl 4-MeO-phenyl 498 499 674 Methoxypropyl 4-HO-phenyl Methyl 4-CF₃-phenyl 536 537 675 Methoxypropyl 4-HO-phenyl Methyl Cyolohexyl 474 475 676 Methoxypropyl 4-HO-phenyl Methyl Benzyl 482 483 677 Methoxypropyl 4-HO-phenyl Methyl

496 497 678 Methoxypropy 4-HO-phenyl Methyl 4-MeO-benzyl 512 513 679 Methoxypropy 4-HO-phenyl Methyl Phenethyl 496 497 680 Methoxypropy 4-HO-phenyl Methyl Pentyl 462 463 681 Methoxypropy 4-HO-phenyl Methyl Hexyl 476 477 682 Phenethyl 4-HO-phenyl Methyl Phenyl 500 501 683 Phenethyl 4-HO-phenyl Methyl 4-Me-phenyl 514 515 684 Phenethyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 528 529 685 Phenethyl 4-HO-phenyl Methyl 4-MeO-phenyl 530 531 686 Phenethyl 4-HO-phenyl Methyl 4-CF₃-phenyl 568 569 687 Phenethyl 4-HO-phenyl Methyl Cyolohexyl 506 507 688 Phenethyl 4-HO-phenyl Metlyl Benzyl 514 515 689 Phenethyl 4-HO-phenyl Methyl

528 529 690 Phenethyl 4-HO-phenyl Methyl 4-MeO-benzyl 544 545 691 Phenethyl 4-HO-phenyl Methyl Phenethyl 528 529 692 Phenethyl 4-HO-phenyl Methyl Pentyl 494 495 693 Phenethyl 4-HO-phenyl Methyl Hexyl 508 509 694 2,2-bisphenylethyl 4-HO-phenyl Methyl Phenyl 576 577 695 2,2-bisphenylethyl 4-HO-phenyl Methyl 4-Me-phenyl 590 591 696 2,2-bisphenylethyl 4-HO-phenyl Methyl 3,5-Me₂-phenyl 604 605 697 2,2-bisphenylethyl 4-HO-phenyl Methyl 4-MeO-phenyl 606 607 698 2,2-bisphenylethyl 4-HO-phenyl Methyl 4-CF₃-phenyl 644 645 699 2,2-bisphenylethyl 4-HO-phenyl Methyl Cyolohoxyl 582 583 700 2,2-bisphenylethyl 4-HO-phenyl Methyl Benzyl 586 587 701 2,2-bisphenylethyl 4-HO-phenyl Methyl

604 605 702 2,2-bisphenylethyl 4-HO-phenyl Methyl 4-MeO-benzyl 620 621 703 2,2-bisphenylethyl 4-HO-phenyl Methyl Phenethyl 604 605 704 2,2-bisphenylethyl 4-HO-phenyl Methyl Pentyl 570 571 705 2,2-bisphenylethyl 4-HO-phenyl Methyl Hexyl 584 585 706 Naphth-1-ylrnethyl Benzyl Methyl Phenyl 520 521 707 Naphth-1-ylmethyl Benzyl Methyl 4-Me-phenyl 534 535 708 Naphth-1-ylrnethyl Benzyl Methyl 3,5-Me₂-phenyl 548 549 709 Naphth-1-ylmethyl Benzyl Methyl 4-MeO-phenyl 550 551 710 Naphth-1-ylrnethyl Benzyl Methyl 4-CF₃-phenyl 588 589 711 Naphth-1-ylrnethyl Benzyl Methyl Cyclohexyl 526 527 712 Naphth-1-ylrnethyl Benzyl Methyl Benzyl 534 535 713 Naphth-1-ylmethyl Benzyl Methyl

548 549 714 Naphth-1-ylmethyl Benzyl Methyl 4-MeO-benzyl 564 565 715 Naphth-1-ylmethyl Benzyl Methyl Phenethyl 548 549 716 Naphth-1-ylrnethyl Benzyl Methyl Pentyl 514 515 717 Naphth-1-ylmethyl Benzyl Methyl Hexyl 528 529 718 Naphth-1-ylrnethyl

Methyl Phenyl 498 499 719 Nephth-1-methyl

Methyl 4-Me-phenyl 512 513 720 Naphth-1-ylmethyl

Methyl 3,5-Me₂-phenyl 526 527 721 Naphth-1-methyl

Methyl 4-MeO-phenyl 528 529 722 Naphth-1-ylmethyl

Methyl 4-CF₃-phenyl 566 567 723 Naphth-1-ylmethyl

Methyl Cyclohexyl 504 505 724 Naphth-1-ylmethyl

Methyl Benzyl 512 513 725 Naphth-1-ylmethyl

Methyl

526 527 726 Naphth-1-ylrnethyl

Methyl 4-MeO-benzyl 542 543 727 Naphth-1-ylrnethyl

Methyl Phenethyl 526 527 728 Naphth-1-ylrnethyl

Methyl Pentyl 492 493 729 Naphth-1-ylmethyl

Methyl Hexyl 506 507 730 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Phenyl 570 571 731 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl 4-Me-phenyl 584 585 732 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl 3,5-Me2-phenyl 598 599 733 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl 4-MeO-phenyl 600 601 734 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl 4-CF₃-phenyl 638 639 735 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Cyclohexyl 576 577 736 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Benzyl 584 585 737 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl

598 599 738 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl 4-MeO-benzyl 614 615 739 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Phenethyl 598 599 740 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Pentyl 564 565 741 Naphth-1-ylmethyl Naphth-1-ylmethyl Methyl Hexyl 578 579 742 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Phenyl 526 527 743 Naphth-1-ylmethyl Cyclohexylmethyl Methyl 4-Me-phenyl 540 541 744 Naphth-1-ylmethyl Cyclohexylmethyl Methyl 3,5-Me₂-phenvl 554 555 745 Naphth-1-ylmethyl Cyclohexylmethyl Methyl 4-MeO-phenyl 556 557 746 Naphth-1-ylmethyl Cyclohexylmethyl Methyl 4-CF₃-phenyl 594 595 747 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Cyolohexyl 532 533 748 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Benzyl 540 541 749 Naphth-1-ylmethyl Cyclohexylmethyl Methyl

554 555 750 Naphth-1-ylmethyl Cyclohexylmethyl Methyl 4-MeO-benzyl 570 571 751 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Phenethyl 554 555 752 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Pentyl 520 521 753 Naphth-1-ylmethyl Cyclohexylmethyl Methyl Hexyl 534 535 754 Naphth-1-ylmethyl 4-chlorobenzyl Methyl Pheny1 554 555 755 Naphth-1-ylmethyl 4-chlorobenzyl Methyl 4-Me-phenyl 568 569 756 Naphth-1-ylmethyl 4-chlorobenzyl Methyl 3,5-Me₂-phenyl 582 583 757 Naphth-1-ylmethyl 4-chlorobenzyl Methyl 4-MeO-phenyl 584 585 758 Naphth-1-ylmethyl 4-chlorobenzyl Methyl 4-CF₃-phenyl 622 623 759 Naphth-1-ylmethyl 4-chlorobenzyl Methyl Cyclobexyl 560 561 760 Naphth-1-ylrnethyl 4-chlorobenzyl Methyl Benzyl 568 569 761 Nephth-1-ylmethyl 4-chlorobenzyl Methyl

582 583 762 Nephth-1-ylmethyl 4-chlorobenzyl Methyl 4-Me-benzyl 598 599 763 Nephth-1-ylmethyl 4-chlorohenzyl Methyl Phenethyl 582 583 764 Nephth-1-ylmethyl 4-chlorobenzyl Methyl Pentyl 548 549 765 Nephth-1-ylmethyl 4-chlorobenzyl Methyl Hexyl 562 563 766 Naphth-1-ylmethyl Methyl Methyl Phenyl 444 445 767 Naphth-1-ylmethyl Methyl Methyl 4-Me-pheny1 458 459 768 Naphth-1-ylmethyl Methyl Methyl 3,5-Me₂-phenyl 472 473 769 Naphth-1-ylmethyl Methyl Methyl 4-MeO-phenyl 474 475 770 Naphth-1-ylmethyl Methyl Methyl 4-CF₃-phenyl 512 513 771 Naphth-1-ylmethyl Methyl Methyl Cyclohexyl 450 451 772 Naphth-1-ylmethyl Methyl Methyl Benzyl 458 459 773 Naphth-1-ylmethyl Methyl Methyl

472 473 774 Naphth-1-ylmethyl Methyl Methyl 4-MeO-benzyl 488 489 775 Naphth-1-ylmethyl Methyl Methyl Phenethyl 472 473 776 Naphth-1-ylmethyl Methyl Methyl Pentyl 438 439 777 Naphth-1-ylmethyl Methyl Methyl Hexyl 452 453 778 Naphth-1-ylmethyl Isobutyl Methyl Phenyl 486 487 779 Naphth-1-ylmethyl Isobutyl Methyl 4-Me-phenyl 500 501 780 Naphth-1-ylmethyl Isobutyl Methyl 3,5-Me₂-phenvl 514 515 781 Naphth-1-ylmethyl Isobutyl Methyl 4-MeO-phenyl 516 517 782 Naphth-1-ylmethyl Isobulyl Methyl 4-CF₃-phenyl 554 555 783 Naphth-1-ylmethyl Isobutyl Methyl Cyclohexyl 492 493 784 Nephth-1-ylmethyl Isobutyl Methyl Benzyl 500 501 785 Naphth-1-ylmethyl Isobulyl Methyl

514 515 786 Naphth-1-ylmethyl Isobutyl Methyl 4-MeO-benzyl 530 531 787 Naphth-1-ylmethyl Isobutyl Methyl Phenethyl 514 515 788 Naphth-1-ylmethyl Isobutyl Methyl Pentyl 480 481 789 Naphth-1-ylmethyl Isobutyl Methyl Hexyl 494 495 790 Naphth-1-ylmethyl Methylthioethyl Methyl Phenyl 504 505 791 Naphth-1-ylmethyl Methylthioethyl Methyl 4-Me-phenyl 518 519 792 Naphth-1-ylmethyl Methylthioethyl Methyl 3,5-Me₂-phenyl 532 533 793 Naphth-1-ylmethyl Methylthioethyl Methyl 4-MeO-phenyl 534 535 794 Nephth-1-ylmethyl Methylthioethyl Methyl 4-CF₃-phenyl 572 573 795 Naphth-1-ylmethyl Methylthioethyl Methyl Cyclohexyl 510 511 796 Naphth-1-ylmethyl Methylthioethyl Methyl Benzyl 518 519 797 Naphth-1-ylmethyl Methylthioethyl Methyl

532 533 798 Naphth-1-ylrnethyl Methylthioethyl Methyl 4-MeO-benzyl 548 549 799 Naphth-1-ylmethyl Methylthioethyl Methyl Phenethyl 532 533 800 Naphth-1-ylmethyl Methylthioethyl Methyl Pentyl 498 499 801 Naphth-1-ylmethyl Methylthioethyl Methyl Hexyl 512 513

In a further aspect of this invention, the present invention provides methods for screening the libraries for bioactivity and isolating bioactive library members.

In yet another aspect, the present invention provides a method for carrying out a binding assay. The method includes providing a composition that includes a first co-activator, an interacting protein, and a test compound. The amino acid structure of the first co-activator includes a binding motif of LXXLL, LXXLI or FxxFF wherein X is any amino acid. The method further includes detecting an alteration in binding between the first co-activator and the interacting protein due to the presence of the compound, and then characterizing the test compound in terms of its effect on the binding.

The assay may be carried out by any means that can measure the effect of a test compound on the binding between two proteins. Many such assays are known in the art and can be utilized in the method of the present invention, including the so-called Two-Hybrid and Split-Hybrid systems.

The Two-Hybrid system, and various means to carry out an assay using this system, are described in, e.g. U.S. Pat. No. 6,410,245. The Split-Hybrid system has been described by, e.g., Hsiu-Ming Shiu et al. Proc. Natl. Acad. Sci. USA, 93:13896-13901, November 1996; and John D. Crispino, at al. Molecular Cell, 3:1-20, February 1999. In the Split-Hybrid system, a fusion protein is utilized where protein X is fused to the lexA DNA binding domains (pLexA) and protein Y is fused to the transcription activator VP16 (pSHM.1-LacZ). Interaction between lexA-X and VP16-Y leads to the expression of the Tetracycline repressor protein (TetR). TetR prevents transcription of the HIS3 reporter gene, making the cells unable to grow on media lacking histidine. Disruption of protein-protein interaction will restore the ability of the cells to grow on such media by shutting down expression of the tetracycline repressor. Accordingly, compounds of the present invention may be added to the growing cells, and if the addition of the compound restores the ability of the cells to grow on the media, the compound may be seen as an effective disruptor of the protein-protein interaction.

The yeast strains required to make the Split-Hybrid system work can be employed with two hybrid LexA/VP16 constructs such as those described by Stanley M. Hollenberg, et al. Molecular and Cellular Biology 15(7):3813-3822, July 1995. A useful modification of the Split-Hybrid system was utilized by Takemaru, K. I. and Moon, R. T. J. of Cell Biol. 149:249-254, 2000.

Other assay formats are also suitable. For example, reporter gene assays for AP-1, ELISA, for example, blocking the production of IL-2 by a T-cell line after stimulation with CD3 and CD28 to look for inhibitors of IL-2 transcription. Direct binding assays (between coactivators and their partners) can be performed by surface plasmon resonance spectroscopy (Biacore, Sweden, manufactures suitable instruments) or ELISA.

Exemplary transcriptional regulators include, without limitation, VP16, VP64, p300, CBP, PCAF, SRC1 PvALF, AtHD2A and ERF-2. See, for example, Robyr et al. (2000) Mol. Endocrinol. 14:329-347; Collingwood et al. (1999) J. Mol. Endocrinol. 23:255-275; Leo et al. (2000) Gene 245:1-11; Manteuffel-Cymborowska (1999) Acta Biochim. Pol. 46:77-89; McKenna et al. (1999) J. Steroid Biochem. Mol. Biol. 69:3-12; Malik et al. (2000) Trends Biochem. Sci. 25:277-283; and Lemon et al. (1999) Curr. Opin. Genet. Dev. 9:499-504. Other exemplary transcription factors include, without limitation, OsGAl, HALF-1, C1, AP1, ARF-5, -6, -7, and -8, CPRF1, CPRF4, MYC-RPIGP, and TRAB1. See, for example, Ogawa et al. (2000) Gene 245:21-29; Okanami et al. (1996) Genes Cells 1:87-99; Goff et al. (1991) Genes Dev. 5:298-309; Cho et al. (1999) Plant Mol. Biol. 40:419-429; Ulmason et al. (1999) Proc. Natl. Acad. Sci. USA 96:5844-5849; Sprenger-Haussels et al. (2000) Plant J. 22:1-8; Gong et al. (1999) Plant Mol. Biol. 41:33-44; and Hobo et al. (1999) Proc. Natl. Acad. Sci. USA 96:15, 348-15,353.

In a preferred embodiment, the transcriptional coactivator is a human transcriptional coactivator. In another preferred embodiment, the transcriptional coactivator is a member of the p300/CBP family of co-activators which have histone acetyltransferase activity. p300 is described for example by Eckner et al, 1994 and CBP by Bannister and Kouzarides, 1996. For the purposes of the present invention, reference to p3001CBP refers to human allelic and synthetic variants of p300, and to other mammalian variants and allelic and synthetic variants thereof, as well as fragments of said human and mammalian forms of p300. In one aspect of the assay, the interacting protein is a transcription factor or a second co-activator.

In one aspect of the assay, the interacting protein is any one of RIP140; SRC-1 (NCoA-1); TIF2 (GRIP-1; SRC-2); p (DP; RAC3; ACTR; A18-1; TRAM-1; SRC-3); CBP (p300); TRAPs (DRIPs); PGC-1; CARM-1; PRIP (ASC-2; AIB3; RAP250; NRC); GT-198; and SHARP (CoAA; p68; p72). In another aspect of the assay, the interacting protein is any one of TAL 1; p73; MDm2; TBP; HIF-1; Ets-1; RXR; p65; AP-1; Pit-1; HNF-4; Stat2; HPV E2; BRCA1; p45 (NF-E2); c-Jun; c-myb; Tax; Sap 1; YY1; SREBP; ATF-1; ATF-4; Cubitus; Interruptus; Gli3; MRF; AFT-2; JMY; dMad; PyLT: HPV E6; CITTA; Tat; SF-1; E2F; junB; RNA helicase A; C/EBP β; GATA-1; Neuro D; Microphthalimia; E1A; TFIIB; p53; P/CAF; Twist; Myo D; pp9O RSK; c-Fos; and SV40 Large T. In another aspect of the assay, the interacting protein is any one of ERAP140; RIP140; RIP160; Trip1; SWI1 (SNF); ARA70; RAP46; TIF1; TIF2; GRIP1; and TRAP. In another aspect of the invention, the interacting protein is any one of VP16; VP64; p300; CBP; PCAF; SRC1 PvALF; AtHD2A; ERF-2; OsGAI; HALF-1: C1; AR-1: ARF-5; ARF-6; ARF-7; ARF-8; CPRF1; CPRF4; MYC-RP/GP; and TRAB1. In another aspect of the invention, the first co-activator is CBP or p300.

The test compound is selected from compounds as described herein. For example, compounds having the formula (I), (II), (III), (IV), (VI) and (VIa). Typically, a test compound will be evaluated at several different concentrations, where these concentrations will be selected, in part, based on the conditions of the assay, e.g., the concentrations of the first co-activator and the interacting protein. Concentrations in the range of about 0.1 to 10 μM are typical. In one aspect, the assay evaluates the relative efficacy of two compounds to affect the binding interaction between two proteins, where at least one of those two compounds is a compound of the present invention. The more effective compound can than serve as a reference compound in a study of the relationship between compound structure and compound activity.

The libraries of the present invention were screened for bioactivity by various techniques and methods. In general, the screening assay may be performed by (1) contacting the mimetics of a library with a biological target of interest, such as a receptor, to allow binding between the mimetics of the library and the target to occur, and (2) detecting the binding event by an appropriate assay, such as the calorimetric assay disclosed by Lam et al. (Nature 354:82-84, 1991) or Griminski et al. (Biotechnology 12:1008-1011, 1994) (both of which are incorporated herein by reference). In a preferred embodiment, the library members are in solution and the target is immobilized on a solid phase. Alternatively, the library may be immobilized on a solid phase and may be probed by contacting it with the target in solution.

Table 4 below shows compounds for bioactivity test selected from the library of the present invention and IC₆₀ values thereof, which are measured by the Reporter gene assay as described in Example 6.

TABLE 4 No STRUCTURE M.W. IC₅₀(μM) 1

580.7 12.8 2

579.6 12.6 3

632.5 13.9 4

617.6 11.8 5

654.6 6.8 6

564.6 6.1 7

564.6 2.2 8

531.6 14.5 9

531.6 6.7 10

531.6 4.0 11

531.6 4.6 12

549.6 9.0 13

549.6 6.4 14

549.6 17.7 15

581.6 4.2 16

567.6 3.8 17

548.0 14.3 18

548.0 3.3 19

582.5 11.5 20

527.6 5.1 21

527.6 5.0 22

543.6 10.4 23

573.6 10.7 24

563.7 5.0 25

581.6 3.0 26

543.6 7.1 27

543.6 5.2 28

548.0 7.5 29

582.5 3.8 30

597.6 7.5 31

613.7 11.9 32

581.6 4.1 33

564.6 13.0 34

565.6 4.4 35

579.7 11.4 36

549.6 12.5 37

545.6 2.3 38

556.7 7.1 39

564.6 9.7 40

553.6 7.0 41

541.6 13.6 42

574.7 18.2 43

556.7 5.2 44

599.6 1.3 45

591.1 2.2 46

570.7 4.4 47

584.7 3.5 48

570.7 10.9 49

592.6 1.4 50

574.6 1.3 51

584.7 4.8 52

621.69 25 53

584.72 9.0 ± 1.5 54

619.16 23.6 ± 5.6  55

584.72 7.2 ± 1.4 56

567.65 9.3 ± 1.6 57

582.70 9.4 ± 1.5 58

588.68 49.1 ± 8.1  59

588.68 5.3 ± 1.3 60

638.69 6.9 ± 1.7 61

570.69 25.8 62

616.73 9.7 ± 1.7 63

582.70 4.1 ± 0.5 64

616.73 25.3 ± 6.6  65

616.73  19 ± 7.1 66

598.74 11.8 67

598.74 6.8 68

590.68 4.3 ± 0.8 69

563.60 1.4 ± 0.7 70

553.62 8.8 ± 1.9 71

596.73 6.5 ± 0.7 72

658.76 3.6 73

658.76 3.6 74

688.74 2.1 ± 0.2 75

568.64 50.5 ± 18.4 76

568.64 10.7 ± 2.5  77

570.67 7.2 ± 2.5 78

570.69 4.3 ± 0.9 79

632.76 16.5 ± 4.8  80

632.76 7.9 ± 2.0 81

607.61 66.1 ± 6.8  82

579.60 68.1 ± 8.9  83

605.14 46.4 ± 3.7  84

740.79 46.7 ± 6.7  85

549.67 15.6 ± 2.2  86

658.76 9.9 ± 2.6 87

624.74 8.1 ± 0.8 88

658.76 2.2 ± 0.2 89

553.62 13.9 ± 0.9  90

647.78 3.9 91

658.76 2.9 ± 0.2 92

658.76 3.8 ± 1.2 93

591.67 6.8 ± 1.3 94

666.78 7.6 ± 0.6 95

564.64 13.3 ± 1.4  96

591.67 8.1 ± 0.9 97

598.70 12.6 ± 1.2  98

666.78 14.4 ± 2.2  99

701.78 2.4 ± 0.3 100

666.78 2.7 ± 0.3 101

666.78 3.9 102

511.58 62.0 ± 17.0 103

535.59 14.5 ± 1.7  104

658.76 4.6 ± 0.4 105

591.67 16.6 ± 2.7  106

591.67 2.6 ± 0.2 107

724.82 2.7 ± 0.3 108

616.67 1.6 ± 0.1 109

616.67 2.1 110

615.13 3.8 ± 0.6 111

587.62 7.2 ± 0.8 112

690.80 4.1 ± 0.8 113

565.57 7.3 ± 1.1 114

588.67  0.4 ± 0.04 115

588.67 0.8 116

570.69 8.0 ± 0.7 117

598.70 6.9 ± 0.6 118

622.72 0.8 ± 0.1 119

551.60 8.8 ± 1.3 120

640.78 34.4 ± 4.9  121

578.67 3.0 ± 0.4 122

592.70 2.1 ± 0.4 123

612.73 11.7 ± 1.0  124

626.75 6.4 ± 0.4 125

619.16 10.3 ±1.5  127

624.74 1.8 ± 0.2 128

590.68 0.4 ± 0.1 129

617.15 2.4 ± 0.5 130

642.75 6.1 ± 0.4 131

666.78 2.2 ± 0.3 132

668.79 2.3 ± 0.5 133

638.77 3.5 ± 0.7 134

636.75 4.5 ± 0.9 135

595.65 2.4 ± 0.7 136

580.65 28.0 ± 2.9  137

625.13 0.6 ± 0.1 138

623.11 1.0 ± 0.2 139

659.18 1.1 ± 0.1 140

657.17 2.7 ± 0.3 141

594.69 1.8 ± 0.3 142

596.71 1.6 ± 0.4 143

575.61 1.3 ± 0.2 144

573.60 2.1 ± 0.2 145

610.71  0.3 ± 0.04 146

608.70 16.7 ± 1.4  147

610.71 9.4 ± 1.0 148

627.14 2.6 ± 0.3 149

639.15 31.0 ± 6.4  150

596.68 12.7 ± 0.7  151

596.68 9.2 ± 0.1 152

622.72 1.2 ± 0.3 153

622.72 1.9 ± 0.3 154

608.74 3.2 ± 0.4 155

680.77 30.5 ± 4.1  156

678.75 13.3 ± 1.6  157

577.63 4.2 ± 0.1 158

610.71  0.9 ± 0.02 159

602.64 2.7 ± 0.2 160

604.66 10.6 ± 0.5  161

741 1.8 ± 0.2 162

618 1.8 ± 0.6 163

742 1.7 ± 0.5 164

539 1.1 ± 0.2 165

565 3.9 ± 0.3 166

565 3.3 ± 0.2 167

624 1.3 ± 0.1 168

541 3.5 ± 0.3 169

734 1.0 ± 0.1 170

575 1.5 ± 0.5 171

617 44.7 ± 6.6  172

566 2.9 ± 0.4 173

690 1.8 ± 0.2 174

664 1.0 ± 0.1 175

594 5.4 ± 0.5 176

578 4.0 ± 0.4 177

590 5.3 ± 0.4 178

576 1.2 ± 0.1 179

645 2.3 ± 0.2 180

609 1.3 ± 0.1 181

592 6.7 ± 0.6 182

597  0.6 ± 0.04 183

554 12.8 ± 0.9  184

554 1.2 ± 0.1 185

639 23.4 ± 1.9  186

576 3.6 ± 0.3 187

598 1.1 ± 0.2 188

590 4.4 ± 0.2 189

639 8.7 ± 0.4 190

639 13.9 ± 0.8  191

639 5.2 ± 0.4 192

583 1.3 ± 0.3 193

569 2.5 ± 0.5 194

667 3.2 ± 0.4 195

564 22.3 ± 2.3  196

613 27.4 ± 2.8  197

721 0.7 ± 0.2 198

613 5.8 ± 0.3 199

660 1.0 ± 0.2 200

568 8.6 ± 0.4 201

628 5.8 ± 0.4 202

584 0.7 ± 0.1 203

598 0.7 ± 0.1 204

667 1.9 ± 0.1 205

582 3.5 ± 0.8 206

624 1.3 ± 0.1 207

609 1.5 ± 0.1 208

570 1.6 ± 0.4 209

694 1.9 ± 0.5 210

694 0.9 ± 0.1 211

694 2.3 ± 0.2 212

694 1.3 ± 0.3 213

694 1.7 ± 0.3 214

694 0.6 ± 0.2 215

639 18 ± 5.1 216

615 1.6 ± 0.2 (1.8 ± 0.3) 217

631 lower than 1.6 218

680 1.6 ± 1.2 219

682 2.2 ± 0.7 220

637 1.1 ± 0.3 221

673 4.7 ± 3.5 222

631 3.8 ± 2.7 223

615 0.6 ± 0.1 224

669 5.4 ± 1.0 225

611 0.1 ± 0.1

It has been found according to the present invention that compounds of general formula (I), and especially the compounds of general formula (VI), can inhibit CBP-mediated transcriptional activation in cancer cells due to their specific binding to CBP. This conclusion is supported by immunoprecipitation of CBP of SW480 cells with compounds of the present invention.

The compounds of the present invention can also inhibit the survivin expression in SW480 cells, and therefore, inhibit the oncogenic activity in cancer cells. The compounds of the present invention can be used for inhibiting cancer cells, and thus, would be useful for the regulation of cell growth. Supporting such results, the compounds of the present invention further shows that it can induce the caspase-3 activation in SW480 cells, and therefore, induce the apoptic activity in cells. The compounds of the present invention can be also advantageously used for inducing apoptosis in cells.

To confirm the oncogenic activity in cancer cell in in vitro MTS cytotoxicity assay was tested by following method.

(1) Cytotoxicity Test

SW480 or HCT116 cells were placed into 96 well microplate (10⁴cells/well) and incubated for 24 hours at 37° C. The cells were treated with TCF4 compound at various concentrations for 24 hours. 20 μl of MTS solution (Promega) was added into each well and incubated for 2 hours at 37° C. Cell viability was measured by reading the absorbance at 490 nm using microplate reader (Molecular Device) and cytotoxicity of a compound at each concentration was calculated.

(2) Growth Inhibition Assay

SW480 or HCT116 cells were placed into 96 well microplate (10⁴ cells/well) and incubated for 24 hours at 37° C. 20 μl of [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt](MTS) solution (Promega) was added into each well and the absorbance after 2 hour incubation at 37° C. (negative control) was read. And then, the cells were treated with TCF4 compound at various concentrations for 48 hours. 20 μl of MTS solution (Promega) was added into each well and incubated for 2 hour at 37° C. Cell viability was measured by reading the absorbance at 490 nm using a microplate reader (Molecular device) and cytotoxicity of a compound at each concentration was calculated.

The results of oncogenic activity for selected library compounds were shown in the Table 5. The compound numbers in Table 5 are unrelated to the compound numbers in Table 4.

TABLE 5 ONCOGENIC ACTIVITY BY MTS OR SULFORHODAMINE B ASSAY FOR SELECTED LIBRARY COMPOUNDS Growth Inhibition (GI50, uM) Compound Structure SW480 HCT116 1

2.28 1.78 2

2.58 2.23 3

2.73 2.39 4

1.99 1.91 5

2.32 2.06 6

3.96 3.91 7

1.22 0.73 8

<0.3 <0.3 9

2.36 1.92 10

2.34 1.66 11

1.97 1.30 12

2.54 1.48 13

1.65 1.59 14

2.70 2.10 15

1.68 1.34 16

4.18 2.95 17

1.12 0.74 18

4.63 3.52 19

2.66 1.17 20

5.02 2.75 21

5.25 1.67 22

6.58 3.26 23

3.9 25.41 24

13.79 1.67 25

24.53 1.81 26

23.89 3.06 27

11.7 1.13 28

3.57 5.47 29

15.98 7.93 30

14.05 5.4 31

8.1 ± 0.7 5.0 ± 1.0 32

47.2 ± 12.1 16.9 ± 1.9  33

ND up to 50 um 28.6 ± 2.0  34

13.8 ± 2.4  5.0 ± 0.7 35

4.7 ± 0.5 5.0 ± 0.7 36

21.9 ± 2.3  12.7 ± 1.3  37

10.4 ± 0.8  9.2 ± 0.9 38

8.5 6.9 39

22.8 ± 6.5  19.7 ± 3.3  40

6.4 ± 0.5 5.8 ± 0.4 41

34.4 ± 9.6  14.7 ± 2.6  42

24.7 10.8 43

ND up to 50 uM 39.1 44

3.8 ± 0.4 4.2 ± 0.5 45

2.5 ± 0.2 2.9 ± 0.4 46

5.5 ± 0.5 9.2 ± 0.9 47

6.2 12.2 48

20.7 ± 2.8  15.5 ± 2.3  49

1.4 ± 0.1 1.0 ± 0.2 50

4.6 2.6 51

3.0 ± 0.1 2.8 52

19.3 ± 2.1  9.7 ± 0.9 53

11.4 ± 0.9  4.7 ± 0.4 54

7.1 ± 0.5 4.9 ± 0.7 55

4.6 ± 0.5 4.1 ± 0.7 56

10.8 9.1 57

3.1 ± 0.3 5.1 ± 0.3 58

47.9 ± 7.2  22.3 ± 4.1  59

ND up to 50 uM 55.1 ± 33.7 60

8.3 ± 1.4 6.3 ± 2.6 61

11.3 ± 6.0  3.6 ± 0.3 62

35.3 ± 4.6 23.5 ± 2.7  63

18.8 ± 4.8 1.3 ± 0.1 64

12.0 ± 0.7  19.0 ± 1.6  65

7.3 4.7 66

3.0 ± 0.3 5.8 ± 0.3 67

0.6 ± 0.2  0.3 ± 0.03 68

3.7 ± 0.2 3.8 ± 0.6 69

17.9 ± 3.1  9.7 ± 1.0 70

7.4 ± 0.6 7.2 ± 0.7 71

4.6 ± 0.5 3.6 ± 0.7 72

10.9 ± 0.6  10.3 ± 1.6  73

9.2 ± 0.8 15.8 ± 2.6  74

1.3 ± 0.4 2.4 ± 0.3 75

2.0 ± 0.1 4.5 ± 0.4 76

4 6.1 77

26.5 ± 6.5  10.7 ± 0.8  78

2.2 ± 0.2 3.7 ± 0.3 79

2.8 ± 0.2 5.2 ± 0.4 80

4.0 ± 0.6 3.9 ± 0.6 81

0.5 ± 0.3 1.8 ± 0.1 82

1.5 1.4 83

2.3 ± 0.3 2.5 ± 0.1 84

8.4 ± 1.1 9.9 ± 1.0 85

1.4 ± 0.5 2.7 ± 0.3 86

9.6 ± 1.6 6.5 ± 0.6 87

0.6 ± 0.2 0.5 ± 0.1 88

0.3 0.4 89

14.6 ± 1.4  7.5 ± 1.0 90

12.6 ± 0.9 14.7 ± 1.0  91

1.5 ± 0.1 3.2 ± 0.2 92

12.9 ± 1.0  14.9 ± 2.2  93

1.9 ± 0.4 1.1 ± 0.1 94

1.1 ± 0.3  0.7 ± 0.07 95

16.2 ± 2.6  7.1 ± 1.2 96

3.7 ± 0.4 3.4 ± 0.4 97

7.1 ± 1.0 5.2 ± 0.5 98

7.0 ± 1.1 4.4 ± 0.5 99

1.0 ± 0.05 0.7 ± 0.1 100

0.3 ± 0.03 0.4 ± 0.1 101

 1.1 ± 0.07 0.9 ± 0.1 102

2.5 ± 0.4 4.9 ± 1.2 103

1.1 ± 0.1 1.5 ± 0.2 104

<0.4 <0.4 105

2.8 ± 0.2 2.1 ± 0.3  106

4.5 ± 0.3 2.8 ± 0.4 107

1.6 ± 0.1 1.6 ± 0.1 108

24.9 ± 2.2  37.9 ± 5.7  109

1.3 ± 0.3 1.1 ± 0.1 110

2.1 ± 0.3 1.9 ± 0.1 111

2.7 ± 0.8 2.1 ± 0.2 112

5.1 ± 0.5 4.7 ± 0.3 113

6.8 ± 1.4 3.7 ± 0.6 114

1.7 ± 0.7 1.9 ± 0.2 115

2.0 ± 0.7  1.1 ± 0.04 116

2.8 ± 0.9 1.7 ± 0.1 117

0.6 ± 0.1  0.3 ± 0.02 118

21.2 ± 1.5 23.2 ± 2.8  119

10.0 ± 1.3  9.5 ± 1.1 120

1.8 ± 0.2 2.6 ± 0.1 121

8.2 ± 0.5 13.1 ± 0.6  122

15.9 ± 5.2  14.8 ± 1.3  123

1.1 ± 0.3 1.7 ± 0.3 124

2.3 ± 0.2 1.4 ± 0.1 125

2.2 ± 0.3 1.9 ± 0.2 126

19.4 ± 3.0  11.6 ± 3.0  127

4.9 ± 0.7 4.3 ± 0.7 128

0.9 ± 0.1  1.0 ± 0.03 129

2.9 ± 0.5 3.1 ± 0.3 130

17.3 ± 1.2  10.7 ± 1.7  131

2.3 ± 0.1 1.7 ± 0.5 132

2.5 ± 0.1 2.2 ± 1.2 133

2.3 ± 0.1 2.1 ± 1.8 134

1.4 ± 0.4 0.8 ± 0.7 135

3.2 ± 0.4 3.1 ± 0.8 136

3.4 ± 0.4 3.0 ± 0.9 137

1.4 ± 0.4 1.3 ± 0.3 138

4.0 ± 0.4 3.9 ± 0.7 139

1.2 ± 0.1 1.0 ± 0.2 140

1.6 ± 0.5 1.7 ± 0.1 141

35 ± 11 21 ± 2.6 142

3.2 ± 0.3 3.3 ± 0.4 143

1.2 ± 0.1 1.2 ± 0.1 144

 0.5 ± 0.03 0.6 ± 0.1 145

6.4 ± 0.1 5.9 ± 0.3 146

3.7 ± 0.5 4.0 ± 0.5 147

6.1 ± 0.4 5.5 ± 0.4 148

1.3 ± 0.1 1.0 ± 0.3 149

2.3 ± 0.1 2.3 ± 0.4 150

1.3 ± 0.1 1.4 ± 0.2 151

11.2 ± 1.3  8.6 ± 0.9 152

0.7 ± 0.1 0.6 ± 0.1 153

12.8 ± 1.6 14.3 ± 7.0  154

0.7 ± 0.2 0.7 ± 0.2 155

26.3 ± 2.5  23.3 ± 1.2  156

3.7 ± 0.3 3.8 ± 0.2 157

1.0 ± 0.2 1.2 ± 0.1 58

4.4 ± 0.1 3.8 ± 0.5 159

9.1 ± 0.5 8.2 ± 0.4 160

13.7 ± 0.5  10.1 ± 01.3 161

4.2 ± 0.4 4.1 ± 0.5 162

1.0 ± 0.3 1.3 ± 0.7 163

2.4 ± 0.2 2.3 ± 0.4 164

3.0 ± 0.3 2.9 ± 0.4 165

22.8 ± 0.9  24.4 ± 1.9  166

27.9 ± 4.7  25.2 ± 3.2  167

 0.3 ± 0.02  0.2 ± 0.02 168

6.2 ± 0.8 6.5 ± 0.3 169

0.8 ± 0.1 1.0 ± 0.2 170

8.9 ± 0.8 8.6 ± 0.8 171

6.2 ± 1.0 6.0 ± 0.4 172

0.8 ± 0.1 0.9 ± 0.1 173

0.6 ± 0.1 0.8 ± 0.1 174

1.9 ± 0.2 1.8 ± 0.1 175

3.0 ± 0.4 2.5 ± 0.1 176

1.7 ± 0.2 1.7 ± 0.1 177

1.8 ± 0.1 1.6 ± 0.1 178

1.6 ± 0.2 1.5 ± 4.4 179

1.5 ± 0.1 1.6 ± 0.1 180

1.0 ± 0.1 1.1 ± 0.1 181

2.3 ± 0.1 2.3 ± 0.1 182

1.0 ± 0.1 0.8 ± 0.1 183

1.6 ± 0.3 1.5 ± 0.1 184

0.7 ± 0.4 0.7 ± 0.1 185

4.9 ± 0.4 4.5 ± 0.2 186

1.7 ± 0.1 2.0 ± 0.2 187

1.0 ± 0.1 1.0 ± 0.1 188

1.6 ± 0.2 1.8 ± 0.2 189

1.0 ± 0.1 1.2 ± 0.1 190

1.1 ± 0.3 1.0 ± 0.1 191

1.2 ± 0.1 1.4 ± 0.1 192

1.1 ± 0.1 1.3 ± 0.1 193

0.8 ± 0.1 1.1 ± 0.1 194

 0.2 ± 0.02  0.2 ± 0.02 195

3.1 ± 0.4 3.0 ± 0.3

In other aspects the present invention provides pharmaceutical compositions containing a compound described herein and a pharmaceutically acceptable carrier. The compounds or compositions of the present invention may be used in various methods (e.g., treating cancer or Alzheimer's disease) of the present invention as described in detail below.

The pharmaceutical composition of the present invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral (e.g., inhalation), transdermal (topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. In addition, pH may be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor EL™ (BASF, Parsippany, N.J.) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incorporating the compound described herein (including both active compounds and prodrugs of the active compounds) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the compound into a sterile vehicle that contains a dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, compound described herein can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and, expectorated or swallowed. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

For administration by inhalation, the compounds are delivered in the form of an aerosol spray from pressured container or dispenser that contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer.

Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the compounds described herein are formulated into ointments, salves, gels, or creams as generally known in the art.

The compounds can also be prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.

In one embodiment, the compounds described herein are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Pat. No. 4,522,811.

It is especially advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals.

Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD50 (the dose lethal to 50% of the population) and the ED50 (the dose therapeutically effective in 50% of the population). The dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD50/ED50. Compounds that exhibit large therapeutic indices are preferred. While compounds that exhibit toxic side effects may be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.

The data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in humans. The dosage of such compounds lies preferably within a range of circulating concentrations that include the ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed and the route of administration utilized. For any compound used in the method of the invention, the therapeutically effective dose can be estimated initially from cell culture assays. A dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC50 (i.e., the concentration of the test compound which achieves a half-maximal inhibition of symptoms) as determined in cell culture. Such information can be used to more accurately determine useful doses in humans. Levels in plasma may be measured, for example, by high performance liquid chromatography.

For instance, in certain embodiments, a pharmaceutical composition of the present invention is one suitable for oral administration in unit dosage form such as a tablet or capsule that contains from about 1 mg to about 1 g of the compound of this invention. In some other embodiments, a pharmaceutical composition of the present invention is one suitable for intravenous, subcutaneous or intramuscular injection. A patient may receive, for example, an intravenous, subcutaneous or intramuscular dose of about 1 μg/kg to about 1 g/kg of the compound of the present invention. The intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection or by continuous infusion over a period of time. Alternatively a patient will receive a daily oral dose approximately equivalent to the daily parenteral dose, the composition being administered 1 to 4 times per day.

The following table illustrates representative pharmaceutical dosage forms containing the compound or pharmaceutically-acceptable salt thereof for therapeutics or prophylactic use in humans:

Tablet 1 mg/tablet Compound 100 Lactose Ph. Eur. 179 Croscarmellose sodium 12.0 Polyvinylpyrrolidone 6 Magnesium stearate 3.0

Tablet 2 mg/tablet Compound 50 Lactose Ph. Eur. 229 Croscarmellose sodium 12.0 Polyvinylpyrrolidone 6 Magnesium stearate 3.0

Tablet 3 mg/tablet Compound 1.0 Lactose Ph. Eur. 92 Croscarmellose sodium 4.0 Polyvinylpyrrolidone 2.0 Magnesium stearate 1.0

Capsule mg/capsule Compound 10 Lactose Ph. Eur. 389 Croscarmellose sodium 100 Magnesium stearate 1.0

Injection I (50 mg/ml) Compound 0.5% w/v Isotonic aqueous solution to 100%

The pharmaceutical composition containing the compound described herein can be used for treatment of disorders modulated by Wnt signaling pathway, especially cancer, more especially colorectal cancer.

In one aspect, the present invention provides compounds that inhibit the binding of a radiolabeled enkephalin derivative to the δ and μ opiate receptors. Accordingly, the reverse-turn mimetics or prodrugs of the present invention may be used as receptor agonists and as potential analgesic agents.

In another aspect, the present invention provides methods for inhibiting tumor growth. Such methods comprise the step of administering to a subject (e.g., a mammalian subject) having a tumor a compound or a composition described herein in an amount effective to inhibit tumor growth. A compound or composition inhibits tumor growth if the tumor sizes are statistically significantly smaller in subjects with the treatment of the compound or composition than those without the treatment.

The inhibitory effect of a particular compound or composition of the present invention on tumor growth may be characterized by any appropriate methods known in the art. For instance, the effect of the compound or composition on survivin expression may be measured. Compounds or compositions down-regulate survivin expression are likely to have inhibitory effects on tumor growth. In addition, assays using tumor cell lines (e.g., soft agar assays using SW480 cells) and animal models for tumor growth (e.g., nude mice grafted with tumor cells and Min mouse model) may also be used to evaluate the inhibitory effect on tumor growth of a given compound or composition as described in detail in the examples. Other exemplary animal models or xenografts for tumor growth include those for breast cancer (Guo et al., Cancer Res. 62: 4678-84, 2002; Lu et al., Breast Cancer Res. Treat. 57: 183-92, 1999), pancreatic cancer (Bouvet et al., Cancer Res. 62: 1534-40, 2002), ovarian tumor (Nilsson et al., Cancer Chemother. Pharmacol. 49: 93-100, 2002; Bao et al., Gynecol. Oncol. 78: 373-9, 2000), melanoma (Demidem et al., Cancer Res. 61: 2294-300, 2001), colorectal cancer (Brown et al., Dig. Dis. Sci. 45: 1578-84, 2000; Tsunoda et al., Anticancer Res. 19: 1149-52, 1999; Cao et al., Clin. Cancer Res 5: 267-74, 1999; Shawler et al., J. Immunother. Emphasis Tumor Immunol. 17: 201-8, 1995; McGregor et al., Dis. Colon. Rectum. 36: 834-9, 1993; Verstijnen et al., Anticancer Res. 8: 1193-200, 1988), hepatocellular cancer (Labonte et al., Hepatol. Res. 18: 72-85, 2000), and gastric cancer (Takahashi et al., Int. J. Cancer 85: 243-7, 2000).

The compound or composition that inhibits tumor growth may be administrated into a subject with a tumor via an appropriate route depending on, for example, the tissue in which the tumor resides. The appropriate dosage may be determined using knowledge and techniques known in the art as described above. The effect of the treatment of the compound or composition on tumor growth may also be monitored using methods known in the art. For instance, various methods may be used for monitoring the progression and/or growth of colorectal cancer, including colonoscopy, sigmoidoscopy, biopsy, computed tomograph, ultrasound, magnetic resonance imaging, and positron emission tomography. Methods for monitoring the progression and/or growth of ovarian cancer include, for example, ultrasound, computed tomography, magnetic resonance imaging, chest X-ray, laparoscopy, and tissue sampling.

In a related aspect, the present invention provides a method for treating or preventing (i.e., reducing the risk of) cancer. Such methods comprise the step of administering to a subject in need thereof a compound or composition described herein in an amount effective to treat or prevent (i.e., reduce the risk of) cancer in the subject. Treating cancer is understood to encompass reducing or eliminating cancer progression (e.g., cancer growth and metastasis). Preventing cancer is understood to encompass preventing or delaying the onset of cancer. Various types of cancer may be treated or prevented by the present invention. They include, but are not limited to, lung cancer, breast cancer, colorectal cancer, stomach cancer, pancreatic cancer, liver cancer, uterus cancer, ovarian cancer, gliomas, melanoma, lymphoma, and leukemia.

In certain embodiments, the method of treating or preventing cancer comprises administering to a subject in need thereof a compound or composition described herein in an amount effective to treat aberrant angiogenesis as described in more detail below.

In certain embodiments, the method of treating or preventing cancer comprises administering to a subject in need thereof a compound or composition described herein in an amount effective to promote apoptosis in the cancer cells as described in more detail below.

In certain embodiments, the method of treating or preventing cancer comprises administering to a subject in need thereof a compound or composition described herein in an amount effective to inhibit survivin expression as described in more detailed below.

A subject in need of treatment may be a human or non-human primate or other animal with various types of cancer. A subject in need of prevention (i.e., reduction of risk) may be a human or non-human primate or other animal that is at risk for developing cancer. Methods for diagnosing cancer and screening for individuals with high risk of cancer are known in the art and may be used in the present invention. For instance, colorectal cancer may be diagnosized by fecal occult blood test, sigmoidoscopy, colonoscopy, barium enema with air contrast, and virtual colonoscopy. An individual with high risk of colorectal cancer may have one or more colorectal cancer risk factors such as a strong family history of colorectal cancer or polyps, a known family history of hereditary colorectal cancer syndromes, a personal history of adenomatous polyps, and a personal history of chronic inflammatory bowel disease.

A compound described herein useful in cancer treatment or prevention (i.e., reduction of risk) may be identified by appropriate methods known in the art. Methods that may be used to select compounds for inhibitory effect on tumor growth as described above may also be used. The route of administration, the dosage of a given compound, the effectiveness of the treatment may be determined using knowledge and techniques known in the art. Factors that may be considered in making such a determination include, for example, type and stage of the cancer to be treated.

The compound described herein useful in cancer treatment and prevention may be administered in combination with an anti-neoplastic agent. An anti-neoplastic agent refers to a compound that inhibits tumor growth. Exemplary anti-neoplastic agents include Fluorouracil; 5-fluoro-2,4(1H, 3H)-pyrimidinedione (5-FU), taxol, cisplatin, mitomycin C, tegafur, raltitrexed, capecitabine, and irinotecan (Arango et al., Cancer Research 61, 2001 4910-4915). A compound administered in combination with an anti-neoplastic agent does not necessarily require that the compound and the anti-neoplastic agent be administered concurrently. The compound and the agent may be administered separately as long as at a time point, they both have effects on same cancer cells.

In a further related aspect, the present invention provides methods for promoting apoptosis in cancer cells. Such methods comprise the step of contacting cancer cells with a compound described herein in an amount effective to promote apoptosis in these cells. A compound promotes apoptosis if the number of cancer cells undergoing apoptosis is statistically significantly larger in the presence of the compound than that in the absence of the compound. Such compounds may be identified by methods known in the art (e.g., measuring caspase activities and/or cell death) using cultured cancer cell lines, xenografts, or animal cancer models. Preferably, the compound is more active in promoting apoptosis in cancer cells than in normal cells. Cancer cells treatable by the present method may be from various tissue origins.

In another aspect of the present invention, a method for treating a disorder modulated by Wnt signaling pathway in which the method comprises administering to a patient a safe and effective amount of the compounds described herein. Pharmaceutical composition containing the compound of the present invention can be also used for this purpose. In this connection, it is found in the present invention that the compounds or pharmaceutical composition described herein can be useful for the treatment of disorder modulated by TCF4-βcatenin-CBP complex, which is believed to be responsible for initiating the overexpression of cancer cells related to Wnt signaling pathway. Thus, it is another aspect of the present invention to provide a method for the treatment of disorder modulated by TCF4-βcatenin-CBP complex, using the compounds described herein.

The present invention also provides compounds and methods for inhibiting survivin expression. Survivin is a target gene of the TCF/beta-catenin pathway, and more specifically is a target gene of the TCF/beta-catenin/CBP pathway. It is a member of the IAP (Inhibitor of Apoptosis Protein) family of proteins. Biological activity associated with survivin includes: highly expressed at G₂/M, regulating cell cycle entry and exit; associated with microtubule, centrosomes, centromeres and midbody depending upon the phases of the cell cycle; and anti-apoptosis via interacting directly or indirectly with caspases (e.g., caspase 3, 7 and 9). In connection with cancer, survivin is widely and highly expressed in tumor cells, but expressed to little or no extent in normal tissue cells. Also, it has been observed that cancer patients whose tumors expressed survivin had a decreased overall survival. Furthermore, the degree of survivin expression has been correlated with other cancer markers, e.g., Ki67, PNCA, p53, APC, etc.

The effect of a particular compound of the present invention on survivin expression may be characterized by methods known in the art. Such methods include methods for characterizing survivin expression at the transcriptional or translational level. Exemplary methods for characterizing survivin expression at the transcriptional level are: cDNA microarray, reverse transcription-polymerase chain reaction (RT-PCR), chromatin immunoprecipitation (ChIP), and assays for reporter activities driven by survivin promoter. Exemplary methods for characterizing survivin expression at the translational level are: Western blot analysis, immunochemistry and caspase activities. Detailed descriptions of the above exemplary methods may be found in the examples below.

As described above, the present invention provides methods for inhibiting survivin expression. Such methods comprise the step of contacting a survivin-expressing cell with a compound of the present invention in an amount effective to inhibit survivin expression. A compound inhibits survivin expression if survivin expression in a cell is decreased in the presence of the compound compared to survivin expression in the absence of the compound. Survivin-expressing cells include tumor cells that express, such as cells in or from lung cancer, breast cancer, stomach cancer, pancreatic cancer, liver cancer, uterus cancer, ovarian cancer, gliomas, melanoma, colorectal cancer, lymphoma and leukemia. The step of contacting the survivin-expressing cells with the compound may be performed in vitro, ex vivo, or in vivo. A compound useful in inhibiting survivin expression may be identified, and the effects of a particular compound of the present invention may be characterized, by appropriate methods known in the art, as described in detail above.

Compounds of the present invention have been shown to inhibit the expression of survivin. Blanc-Brude et al., Nat. Medicine 8:987 (2002), have shown that survivin is a critical regulator of smooth muscle cell apoptosis which is important in pathological vessel-wall remodeling. Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) restenosis associated with angioplasty comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the restenosis, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having restenosis achieves a reduction in the severity, extent, or degree, etc. of the restenosis. In another embodiment the invention prevents (i.e., reduces the risk of) the restenosis, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional restenosis achieves a reduction in the anticipated severity, extent, or degree, etc. of the restenosis. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit TCF/B-catenin transcription. Rodova et al., J. Biol. Chem. 277:29577 (2002), have shown that PKD-1 promoter is a target of the B-catenin/TCF pathway. Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) polycystic kidney disease comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the polycystic kidney disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having polycystic kidney disease achieves a reduction in the severity, extent, or degree, etc. of the polycystic kidney disease. In another embodiment the invention prevents (i.e., reduces the risk of) polycystic kidney disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional polycystic kidney disease achieves a reduction in the anticipated severity, extent, or degree, etc. of the polycystic kidney disease. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit the expression of Wnt signaling. Hanai et al., J. Cell Bio. 158:529 (2002), have shown that endostatin, a known anti-angiogenic factor, inhibits Wnt signaling. Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) aberrant angiogenesis disease comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the aberrant angiogenesis disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having aberrant angiogenesis disease achieves a reduction in the severity, extent, or degree, etc. of the aberrant angiogenesis disease. In another embodiment, the invention prevents (i.e., reduces the risk of) aberrant angiogenesis disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional aberrant angiogenesis disease achieves a reduction in the anticipated severity, extent, or degree, etc. of the aberrant angiogenesis disease. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit the expression of Wnt signalling. Sen et al., P.N.A.S. (USA) 97:2791 (2000), have shown that mammals with rheumatoid arthritis demonstrate increased expression of Wnt and Fz in RA synovial tissue. Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) rheumatoid arthritis disease comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the rheumatoid arthritis disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having rheumatoid arthritis disease achieves a reduction in the severity, extent, or degree, etc. of the rheumatoid arthritis disease. In another embodiment the invention prevents (i.e., reduces the risk of) rheumatoid arthritis disease, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional rheumatoid arthritis disease achieves a reduction in the anticipated severity, extent, or degree, etc. of the rheumatoid arthritis disease. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit the expression of Wnt signalling. Uthoff et al., Int. J. Oncol. 19:803 (2001), have shown that differential upregulation of disheveled and fz (Wnt pathway molecules) occurs in ulcerative colitis (compared to Chron's disease patients). Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) ulcerative colitis comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the ulcerative colitis, Le., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having ulcerative colitis achieves a reduction in the severity, extent, or degree, etc. of the ulcerative colitis. In another embodiment the invention prevents (i.e., reduces the risk of) ulcerative colitis, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional ulcerative colitis achieves a reduction in the anticipated severity, extent, or degree, etc. of the ulcerative colitis. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit Wnt TCF/catenin signalling. Accordingly, another aspect of the invention provides a method of treating or preventing (i.e., reducing the risk of) tuberious sclerosis complex (TSC) comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. Subjects having TSC typically develop multiple focal lesions in the brain, heart, kidney and other tissues (see, e.g., Gomez, M. R. Brain Dev. 17(suppl): 55-57 (1995)). Studies in mammalian cells have shown that overexpression of TSC1 (which expresses hamartin) and TSC2 (which expresses tuberin) negatively regulates cell proliferation and induces G₁/S arrest (see, e.g., Miloloza, A. et al., Hum. Mol. Genet. 9: 1721-1727 (2000)). Other studies have shown that hamartin and tuberin function at the level of the β-catenin degradation complex, and more specifically that these proteins negatively regulate beta-catenin stability and activity by participating in the beta-catenin degradation complex (see, e.g., Mak, B. C., et al. J. Biol. Chem. 278(8): 5947-5951, (2003)). Beta-catenin is a 95-kDa protein that participates in cell adhesion through its association with members of the membrane-bound cadherin family, and in cell proliferation and differentiation as a key component of the Wnt/Wingless pathway (see, e.g., Daniels, D. L., et al., Trends Biochem. Sci. 26: 672-678 (2001)). Misregulation of this pathway has been shown to be oncogenic in humans and rodents. The present invention provides compounds that modulate β-catenin activity, and particularly its interactions with other proteins, and accordingly may be used in the treatment of TSC. Thus, in one embodiment the invention treats TSC, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having TSC achieves a reduction in the severity, extent, or degree, etc. of the TSC. In another embodiment the invention prevents (i.e., reduces the risk of) TSC, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional TSC achieves a reduction in the anticipated severity, extent, or degree, etc. of the TSC. Optionally, the subject is a mammalian subject.

Compounds of the present invention have been shown to inhibit the expression of Wnt signalling. The Kaposi's sarcoma-associated herpesvirus (KSHV) latency-associated nuclear antigen (LANA) is expressed in all KSHV-associated tumors, including Kaposi's sarcoma (KS) and β-cell malignancies such as primary effusion lymphoma (PEL) and multicentric Castleman's disease. Fujimuro, M. et al., Nature Medicine 9(3):300-306 (2003), have shown that LANA acts to stabilize β-catenin, apparently by redistribtution of the negative regular GSK-3 β. The present invention provides compounds and methods for inhibiting β-catenin protein interactions, e.g., β-catenin/TCF complex formation. Thus, the compounds of the present invention thwart the LANA-induced accumulation of β-catenin/TCF complex and, at least in part, the consequences of KSHV infection. Accordingly, another aspect of the present invention provides a method of treating or preventing (i.e., reducing the risk of) conditions due to infection by Karposi's sarcoma-associated herpesvirus (KSHV). Such conditions include KSHV-associated tumors, including Kaposi's sarcoma (KS) and primary effusion lymphoma (PEL). The method comprises administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention. In one embodiment the invention treats the KSHV-associated tumor, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject having a KSHV-associated tumor achieves a reduction in the severity, extent, or degree, etc. of the tumor. In another embodiment the invention prevents (i.e., reduces the risk of) a KSHV-associated tumor, i.e., administration of a reverse-turn mimetic or prodrug of the present invention to a subject that is anticipated to develop new or additional KSHV-associated tumors achieves a reduction in the anticipated severity, extent, or degree, etc. of the tumor. Optionally, the subject is a mammalian subject.

LEF/TCF DNA-binding proteins act in concert with activated β-catenin (the product of Wnt signaling) to transactivate downstream target genes. DasGupta, R and Fuchs, E. Development 126(20):4557-68 (1999) demonstrated the importance of activated LEF/TCF complexes at distinct times in hair development and cycling when changes in cell fate and differentiation commitments take place. Furthermore, in skin morphogenesis, β-catenin has been shown to be essential for hair follicle formation, its overexpression causing the “furry” phenotype in mice (Gat, U., et al. Cell 95:605-614 (1998) and Fuchs, E. Harvey Lect. 94:47-48 (1999). See also Xia, X. et al. Proc. Natl. Aad. Sci. USA 98:10863-10868 (2001). Compounds of the present invention have been shown to inhibit the expression of Wnt signaling, and interfere with formation of β-catenin complexes. Accordingly, the present invention provides a method for modulating hair growth comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention, where the amount is effective to modulate hair growth in the subject. Optionally, the subject is a mammalian subject.

The present invention provides compounds useful in treating or preventing (i.e., reducing the risk of) Alzheimer's disease. Alzheimer's disease (AD) is a neurodegenerative disease with progressive dementia. This disease is accompanied by three main structural changes in the brain, namely, i) intracellular protein deposits (also known as neurofibrillary tangles, or NFT), ii) extracellular protein deposits termed amyloid plaques that are surrounded by dystrophic neuritis, and iii) diffuse loss of neurons.

The compounds or compositions of the present invention rescue defects in neuronal differentiation caused by a presenilin-1 mutation and may decrease the number, or rate at which neuronal precursor populations differentiate to neurons in Alzheimer's brains. Presenilins are transmembrane proteins whose functions are related to trafficking, turnover and cleavage of Notch and Amyloid Precursor Protein. Missense mutations in presenilin 1 (PS-1) are associated with early-onset familial Alzheimer's disease (Fraser et al., Biochem. Soc. Symp. 67, 89 (2001)). The compounds of the present invention may be applicable not only to individuals with PS-1 familial Alzheimer's mutations, but also to general Alzheimer's patients.

In addition, the present invention provides a method for treating or preventing Alzheimer's disease comprising administering to a subject in need thereof a safe and effective amount of a reverse-turn mimetic or prodrug of the present invention, where the amount is effective to treat or prevent (i.e. reduce the risk of) Alzheimer's disease in the subject. Treating Alzheimer's disease is understood to encompass reducing or eliminating the manifestation of symptoms characteristic of Alzheimer's disease, or delaying the progression of this disease. Preventing Alzheimer's disease is understood to encompass preventing or delaying the onset of this disease.

A subject in need of treatment may be a human or non-human primate or other animal that is at various stages of Alzheimer's disease. Methods for diagnosing Alzheimer's disese are known in the art (see, e.g., Dinsmore, J. Am. Osteopath. Assoc. 99(9 Suppl.):S1-6, 1999; Kurz et al., J. Neural Transm. Suppl. 62: 127-33, 2002; Storey et al., Front Viosci. 7: e155-84, 2002; Marin et al., Geriatrics 57: 36-40, 2002; Kril and Halliday, Int. Rev. Neurobiol. 48: 167-217, 2001; Gurwitz, Trends Neurosci. 23: 386, 2000; Muller-Spahn and Hock, Eur. Arch. Psychiatry Clin. Neurosci. 249 Suppl. 3: 37-42; Fox and Rossor, Rev. Neuro. (Paris) 155 Suppl. 4: 533-7, 1999), including the use of neuropsychological measures, functional imaging measures, biological markers, and autopsy of brain tissue. A subject in need of prevention (i.e., reduction of risk) may be a human or non-human primate or other animal that is at risk for developing Alzheimer's disease, such as an individual having a mutation of certain genes responsible for this disease (e.g., genes encoding amyloid precursor protein, presenilin 1, and presenilin 2), and/or a gene involved in the pathogenesis of this disease (e.g., apolipoprotein E gene) (Rocchi et al., Brain Res. Bull. 61: 1-24, 2003).

Compounds with structures as set forth in formula (I) may be screened for their activities in treating or preventing Alzheimer's disease by any appropriate methods known in the art. Such screening may be initially performed using in vitro cultured cells (e.g., PC-12 cells as described in Example 8). Compounds capable of rescuing defects in neuronal differentiation caused by a presenilin 1 mutation may be further screened using various animal models for Alzheimer's disease. Alternatively, compounds with structures as set forth in formula (I) may be directedly tested in animal models for Alzheimer's disease. Many model systems are known in the art and may be used in the present invention (see, e.g., Rowan et al., Philos. Trans. R. Soc. Lond. B. Biol. Sci. 358: 821-8, 2003; Lernere et al., Neurochem. Res. 28: 1017-27, 2003; Sant'Angelo et al., Neurochem. Res. 28: 1009-15, 2003; Weiner Harv. Rev. Psychiatry 4: 306-16, 1997). The effects of the selected compounds on treating or preventing Alzheimer's disease may be characterized or monitored by methods known in the art for evaluating the progress of Alzheimer's disease, including those described above for diagnosing this disease.

The present invention also provides methods for promoting neurite outgrowth. Such methods comprise the step of contacting a neuron with a compound described herein in an amount effective to promote neurite outgrowth. These methods are useful in treating neurodegenerative diseases (e.g., glaucoma, macular degeneration, Parkinson's Disease, and Alzheimer's disease) and injuries to nervous system. A compound promotes neurite outgrowth if the neurite lengths of neurons are statistically significantly longer in the presence of the compound than those in the absence of the compound. Such a compound may be identified using in vitro cultured cells (e.g, PC-12 cells, neuroblastoma B104 cell) (Bitar et al., Cell Tissue Res. 298: 233-42, 1999; Pellitteri at al., Eur J. Histochem. 45: 367-76, 2001; Satoh et al., Biochem. Biophys. Res. Commun. 258: 50-3, 1999; Hirata and Fujisawa, J. Neurobiol. 32:415-25, 1997; Chauvet et al., Glia 18: 211-23, 1996; Vetter and Bishop, Curr. Biol. 5: 168-78, 1994; Koo at al., Proc. Natl. Acad. Sci. USA 90: 4748-52, 1993; Skubitz et al., J. Cell Biol. 115: 1137-48, 1991; O'Shea et al., Neuron 7: 231-7, 1991; Rydel and Greene, Proc. Natl. Acad. Sci. USA 85: 1257-61, 1988) or using explants (Kato et al.; Brain Res 31: 143-7, 1983; Vanhems at al., Eur J. Neurosci. 2: 776-82, 1990; Carri at al., Int J. Day. Neurosci. 12: 567-78, 1994). Contacting a neuron with a compound according to the present invention may be carried out in vitro or in vivo. The resulting treated neuron, if generated in vitro, may be transplanted into a tissue in need thereof (Lacza et al., Brain Res. Brain Res. Protoc. 11: 145-54, 2003; Chu et al., Neurosci. Lett 343: 129-33, 2003; Fukunaga at al., Cell Transplant 8: 435-41 1999).

The present invention also provides methods for promoting differentiation of a neural stem cell comprising contacting a neural stem cell with a compound described herein in an amount effective to promote differentiation of a neural stem cell. Such methods are also useful in treating neurodegenerative diseases (e.g., glaucoma, macular degeneration, Parkinson's Disease, and Alzheimer's disease) and injuries to nervous system. “Neural stem cell” refers to a clonogenic, undifferentiated, multipotent cell capable of differentiating into a neuron, an astrocyte or an oligodendrocyte under appropriate conditions. A compound promotes differentiation of neural stem cells if neural stem cells exhibit a statistically significantly higher degree of differentiation in the presence of the compound than in the absence of the compound. Such a compound may be identified using assays involving in vitro cultured stem cells or animal models (Albranches et al., Biotechnol. Lett. 25: 725-30, 2003; Deng et al., Exp. Neurol. 182: 373-82, 2003; Munoz-Elias et al., Stem Cells 21: 437-48, 2003; Kudo et al., Biochem. Pharmacol. 66: 289-95, 2003; Wan et al., Chin. Med. J. 116: 428-31, 2003; Kawamorita et al., Hum. Cell 15: 178-82, 2002: Stpyridis and Smith, Biochem. Soc. Trans, 31: 45-9, 2003; Pachernik et al., Reprod. Nutr. Dev. 42: 317-26, 2002; Fukunaga et al., supra). The neural stem cell may be a cultured stem cell, a stem cell freshly isolated from its source tissue, or a stem cell within its source organism. Thus, contacting the neural stem cell with a compound according to the present invention may be carried out either in vitro (for a cultured or freshly isolated stem cell) or in vivo (for a stem cell within its source organism). The resulting differentiated neural cell, if generated in vitro, may be transplanted into a tissue in need thereof (Lacza et al., supra; Chu et al., supra; Fukunaga et al., supra). Such a tissue includes a brain tissue or other nervous tissue that suffers from a trauma or a neurodegenerative disease.

In certain embodiments, the methods for promoting differentiation of a neural stem cell comprising contacting a neural stem cell with a compound described herein in an amount effective to promote neurite outgrowth as described in more detail above.

The following non-limiting examples illustrate the compounds, compositions, and methods of use of this invention.

EXAMPLES Preparation Example 1 Preparation of (N-Fmoc-N′—R₃-hydrazino)-acetic acid (1) Preparation of N-Fmoc-N′-Methyl Hydrazine

2 L, two-neck, round-bottomed-flask was fitted with a glass stopper and a calcium tube. A solution of methylhydrazine sulfate (20 g, 139 mmol, where R₃ is methyl) in THF (300 mL) was added and a solution of DiBoc (33 g, 153 mmol) in THF was added. Saturated sodium bicarbonate aqueous solution (500 mL) was added dropwise via addition funnel over 2 hours with vigorous stirring. After 6 hours, a solution of Fmoc-Cl (39 g, 153 mmol) in THF was added slowly. The resulting suspension was stirred for 6 hours at 0° C. The mixture was extracted with ethyl acetate (EA, 500 mL) and the organic layer was retained. The solution was dried with sodium sulfate and evaporated in vacuo. The next step proceeded without purification.

A 1 L, two-necked, round-bottom-flask was fitted with a glass stopper and a calcium tube. A solution of the product from the previous step in MeOH (300 mL) was added and conc. HCl (30 mL, 12 N) was added slowly via addition funnel with magnetic stirring in ice water bath and stirred overnight. The mixture was extracted with EA (1000 mL) and the organic layer was retained. The solution was dried with sodium sulfate and evaporated in vacuo. The residue was purified by recrystallization with n-hexane and EA to give N-Fmoc-W-methyl hydrazine (32.2 g, 83%). ¹HNMR (DMSO-D6) δ 7.90˜7.88 (d, J=6 Hz, 2H), δ 7.73˜7.70 (d, J=9 Hz, 2H), 7.44˜7.31 (m, 4H), 4.52˜4.50 (d, J=6 Hz, 2H), 4.31˜4.26 (t, J=6 Hz, 1H), 2.69 (s, 1H).

(2) Preparation of N-Fmoc-N′-methyl-hydrazino)-acetic acid t-butyl ester

1 L, two-necked, round-bottom-flask was fitted with a glass stopper and reflux condenser connected to a calcium tube. A solution of N-Fmoc-N′-methyl hydrazine (20 g, 75 mmol) in toluene (300 mL) was added. A solution of butylbromo acetate (22 g, 111 mmol) in toluene (50 mL) was added slowly. Cs₂CO₃ (49 g, 149 mmol) was added slowly, NaI (11 g, 74 mmol) was added slowly with vigorous stirring. The reaction mixture was stirred at reflux temperature over 1 day. The product mixture was filtered and extracted with EA (500 mL). The solution was dried over sodium sulfate and evaporated in vacuo. The product was purified by chromatography with hexane:EA=2:1 solution to give (N-Fmoc-N′-methyl-hydrazino)-acetic acid t-butyl ester (19.8 g, 70%).

¹H-NMR (CDCl₃-d) δ 7.78˜7.75 (d, J=9 Hz, 2H), δ 7.61˜7.59 (d, J=6 Hz, 2H), 7.43˜7.26 (m, 4H), 4.42˜4.40 (d, J=6 Hz, 2H), 4.23 (b, 1H), 3.57 (s, 2H), 2.78 (s, 3H), 1.50 (s, 9H).

(3) Preparation of N-Fmoc-N′-methyl-hydrazino)-acetic acid

1 L, two-neck, round-bottomed-flask was fitted with a glass stopper and reflux condenser connected to a calcium tube. (N-Fmoc-N′-methyl-hydrazino)-acetic acid t-butyl ester (20 g, 52 mmol) was added. A solution of HCl (150 mL, 4 M solution in dioxane) was added slowly with vigorous stirring in an ice water bath. The reaction mixture was stirred at RT over 1 day. The solution was concentrated completely under reduced pressure at 40° C. A saturated aq. NaHCO₃ solution (100 mL) was added and the aqueous layer was washed with diethyl ether (100 mL). Conc. HCl was added dropwise slowly at 0° C. (pH 2-3). The mixture was extracted and the organic layer was retained (500 mL, MC). The solution was dried with sodium sulfate and evaporated in vacuo. The residue was purified by recrystallization with n-hexane and ethyl acetate to give (N-Fmoc-N′-methyl-hydrazino)-acetic acid (12 g, 72%). ¹H-NMR (DMSO-d₈) δ 12.38 (5, 1H), 8.56 (b, 1H), 7.89˜7.86 (d, J=9 Hz, 2H), 7.70˜7.67 (d, J=9 Hz, 2H), 7.43˜7.29 (m, 4H), 4.29˜4.27 (d, J=6 Hz, 2H), 4.25˜4.20 (t, J=6 Hz, 1H), 3.47 (s, 2H), 2.56 (s, 3H).

Preparation Example 2 Preparation of (N-Moc-N′—R₇-hydrazino)-acetic acid (1) Preparation of (N′-Methoxycarbonyl-hydrazino)-acetic acid ethyl ester

MOC—NH—NH₂ (50 g, 0.55 mol) was dissolved in DMF (300 ml), and then ethyl bromoacetate (68 ml, 0.555 mol) and potassium carbonate (77 g, 0.555 mol) were added to the reaction vessel. The mixture was warmed to 50° C. for 5 hours. After the reaction was completed, the mixture was filtered, and diluted with EtOAc, and washed with brine (3 times). The crude product was purified by column (eluent: Hex/EtOAc=4/1) to provide 72 of colorless oil.

(2) [N—R₇—N′-methoxycarbonyl-hydrazino]-acetic acid ethyl ester

The ethyl ester (10 g, 0.05 mol), potassium carbonate (6.9 g, 0.05 mol), and R₇-bromide (14.1 g, 0.06 mol) were dissolved in DMF (200 ml), and The mixture was warmed to 50° C. for 5 hours. After the reaction was completed, the mixture was filtered, and diluted with EA, and washed with brine (3 times). The crude product was purified by Chromatography (eluent Hex/EtOAc=4/1).

(3) [N—R₇—N′-methoxycarbonyl-hydrazino]-acetic acid

The alkylated ethyl ester (9.5 g, 0.03 mol) was dissolved in THF/water (1/1, ml), and added 2N NaOH (28.3 ml) solution at 0° C. The mixture was stirred at RT for 2 hours. After the starting ester was not detected on UV, the solution was diluted with EA, then separated. The aqueous layer was acidified to pH 3˜4 by 1N HO, and the compound was extracted by DCM (3 times). The combined organic layer was dried over MgSO4, and evaporated to give a yellow solid.

Preparation Example 3 (1) Preparation of Benzyl-(2,2-diethoxy-ethyl)-amine

To a solution of Benzaldehyde (1.27 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.75 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (816 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of [1-[Benzyl-(2,2-diethoxy-ethyl-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of Benzyl-(2,2-diethoxy-ethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and Ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to give [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (4.3 g, 2 step yield: 62%). MS ESI 577 (M+H)

(3) Preparation of 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amide

To a solution of [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (3.32 g, 5.76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-N-benzyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide, which was used next step without further purification.

To a solution of 2-Amino-N-benzyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide in CH₂Cl₂(50 ml) was added a solution of (3R)-3-(3-Benzyl-ureido)-hex-5-enoic acid (1.6 g, 6.1 mmol), EDCl (1.17 g, 7.3 mmol, 1.2 eq), HOBt (0.93 g, 7.3 mmol, 1.2 eq), DIEA (2.13 mL, 12.2 mmol 2.4 eq) in CH₂Cl₂ (100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 687 (M+H), 709 (M+Na)

(4) Preparation of 2-Allyl-8-benzyl-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amide (2.9 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and Hexane to give the 2-Allyl-8-benzyl-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.18 g, 3 step yield: 38%). ¹H NMR (CDCl₃, 300 MHz) δ 7.5˜7.26 (m, 5H), 7.25 (d, J=7.01, 2H), 6.85 (m, 5H), 6.55 (d, J=8.76, 2H), 5.7 (m, 1H), 5.3 (t, J=4.7, 1H), 5.05 (d, J=10.75, 1H), 5.0 (d, J=18.54, 1H), 4.87 (d, J=14.51, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H, OH), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.6˜2.4 (m, 2H), 2.2 (t, J=7.2, 2H) MS ESI 539 (M+H), 561 (M+Na).

Preparation Example 4 (1) Preparation of Benzyl-(2,2-diethoxy-ethyl)-amine

To a solution of Benzaldehyde (1.27 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.75 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (816 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester

To a solution of Cbz-T (O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of Benzyl-(2,2-diethoxy-ethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to give [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (4.3 g, 2 step yield: 69%). MS ESI 577 (M+H)

(4) Preparation of N-[1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-4-tert-butoxy-phenyl)-ethyl]-3-(3-benzyl-ureido)-butyramide

To a solution of [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert butoxy-phenyl)-ethyl]carbamic acid benzyl ester (332 g, 5. 76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-N-benzyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide, which was used next step without further purification.

To a solution of 2-Amino-N-benzyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide in CH₂Cl₂(50 ml) was added a solution of (3R)-3-(3-Benzyl-ureido)-butyric acid (1.44 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mmol) in CH₂Cl₂(100 ml) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 661 (M+H), 683(M±Na)

(4) Preparation of 8-Benzyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amine (3.26 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 8-Benzyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.12 g, 3 step yield: 38%), ¹H NMR (CDCl₃, 300 MHz) δ 7.5˜7.3 (m, 5H), 7.2 (d, J=7.01, 2H), 6.80 (m, 5H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H, OH), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H) 2.2 (t, J=7.2, 2H) 1.36 (m, 3H) MS ESI 513(M+H), 535 (M+Na).

Example 5 (1) Preparation of 2-Allyl-8-(2,3-dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

To a solution of 2,3-dimethoxybenzaldehyde (2 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.49 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (829 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-2,3-dimethoxy-benzyl]-carbamoyl}-ethyl}-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of 2-Allyl-8-(2,3-dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to gave the compound (4.3 g, 2 step yield: 69%). MS ESI 730.50 (100% M+H)

(5) Preparation of 3-(3-Benzyl-ureido)-hex-5-enoic acid {2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-carbamoyl]-ethyl}-amide

To a solution of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-2, dimethoxy-benzyl]-carbamoyl}-ethyl}-carbamic acid benzyl ester (3.67 g, 5.76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford the 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy)-N-(2,3-dimethoxy-benzyl)-propionamide which was used next step without further purification.

To a solution of 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy)-N-(2,3-dimethoxy-benzyl)-propionamide in CH₂Cl₂ (50 ml) was added a solution of 3-(3-Benzyl-ureido)-hex-5-enoic acid (1.6 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mL) in CH₂Cl₂(100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 747.65 (80% M+H), 769.45 (30% M+Na)

(4) Preparation of 2-Allyl-8-(2,3-dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic benzylamide

A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid {2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-carbamoyl]-ethyl}-amide (3.7 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 2-Allyl-8-(2,3-dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic benzylamide (1.3 g, 3 step yield: 38%). ¹H NMR (CDCl₃, 300 MHz) δ 7.4˜7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.85 (m, 3H), 6.8 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 5.05 (d, J=10.75, 1H) 5.0 (d, J=18.54, 1H), 4.87 (d, J=14.51, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H, OH), 3.82 (s, 3H), 3.66 (s, 3H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.6˜2.4 (m, 2H), 2.2 (t, J=7.2, 2H) MS ESI 599.32 (M+H), 621.38 (M+Na), 637.19 (M+K)

Preparation Example 6 (1) Preparation of (2,2-Diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-amine

To a solution of 2,3-dimethoxybenzaldehyde (2 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.49 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (829 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-2,3-dimethoxy-benzyl]-carbamoyl}-ethyl}-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of (2,2-Diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to gave the compound (4.3 g, 2 step yield 69 MS ESI 730.50 (M+H)

(6) Preparation of 3-(3-Benzyl-ureido)-N-{2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-carbamoyl]-ethyl}-butyramide

To a solution of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-2,3-dimethoxy-benzyl]-carbamoyl}ethyl}-carbamic acid benzyl ester (3.67 g, 5.76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford the 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy)-N-(2,3-dimethoxy-benzyl)-propionamide which was used next step without further purification.

To a solution of 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy)-N-(2,3-dimethoxy-benzyl)-propionamide in CH₂Cl₂(50 mL) was added a solution of (3R)-3-(3-Benzyl-ureido)-butyric acid (1.44 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mmol) in CH₂Cl₂ (100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 721 (M+H), 743 (M+Na)

(4) Preparation of 8-(2,3-Dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-N-{2-(4-tert-butoxy-phenyl)-1-[(2,2,-diethoxy-ethyl)-(2,3-dimethoxy-benzyl)-carbamoyl]-ethyl}-butyramide (3.56 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 8-(2,3-Dimethoxy-benzyl)-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.32 g, 3 step yield: 40%). ¹H NMR (CDCl₃, 300 MHz) δ 7.4˜7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.85 (m, 3H), 6.8 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H, OH), 3.82 (s, 3H), 3.66 (s, 3H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.2 (t, J=7.2, 2H) 1.45 (m, 3H) MS ESI 573 (M+H), 595 (M+Na).

Preparation Example 7 (1) Preparation of (2,2-Diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-amine

To a solution of 1H-indazole-7-carbaldehyde (1.75 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.74 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (816 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl-carbamoyl]-ethyl}-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of (2,2-Diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to gave {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-carbamic acid benzyl ester (5.1 g, 2 step yield: 69%). MS ESI 617 (M+H)

(7) Preparation of 3-(3-Benzyl-ureido)-hex-5-enoic acid {2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-amide

To a solution of [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert butoxy-phenyl)-ethyl]carbamic acid benzyl ester (3.54 g, 5.76 mmol) in MeOH (50 ml) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-N-(1H-indazol-7-ylmethyl)-propionamide, which was used next step without further purification.

To a solution of 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-N-(1H-indazol-7-ylmethyl)-propionamide in CH₂Cl₂ (50 mL) was added a solution of (3R)-3-(3-Benzyl-ureido)-hex-5-enoic acid (1.6 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mmol) in CH₂Cl₂(100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 727 (M+H), 749 (M+Na)

(4) Preparation of 2-Allyl-6-(4-hydroxy-benzyl)-8-(1H-indazol-7-ylmethyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid {2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-amide (3.60 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 2-Allyl-6-(4-hydroxy-benzyl)-8-(1H-indazol-7-ylmethyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.0 g, 3 step yield: 30%), ¹H NMR (CDCl₃, 300 MHz) δ 8.20 (s, 1H), 7.4-7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.80 (m, 3H), 6.75 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 5.05 (d, J=10.75, 1H), 5.0 (d, J=18.54, 1H), 4.87 (d, J=14.51, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.6˜2.4 (m, 2H), 2.2 (t, J=7.2, 2H) MS ESI 579 (M+H), 601 (M+Na).

Preparation Example 8 (1) Preparation of (2,2-Diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-amine

To a solution of 1H-Indazole-7-carbaldehyde (175 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.74 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (816 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of {2-(4-tert-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of (2,2-Diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to give {2-(4-tent-Butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-1-indazol-7-ylmethyl)-carbamoyl]-ethyl}-carbamic acid benzyl ester (5.1 g, 2 step yield: 69%). MS ESI 617 (M+H).

(3) Preparation of 3-(3-Benzyl-ureido)-N-{2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-butyramide

To a solution of [1-[Benzyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (3.54 g, 5.76 mmol) in MeOH (50 mL) was added. Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-N-(1H-indazol-7-ylmethyl)-propionamide which was used next step without further purification.

To a solution of 2-Amino-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-N-(1H-indazol-7-ylmethyl)-propionamide in CH₂Cl₂ (50 mL) was added a solution of (3R)-3-(3-Benzyl-ureido)-butyric acid (1.44 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mmol) in CH₂Cl₂ (100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated zin vacuo. The crude compound was used next step without further purification. MS ESI 701 (M+H), 723 (M+Na).

(4) Preparation of 6-(4-Hydroxy-benzyl)-8-(1H-indazol-7-ylmethyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-N-{2-(4-tert-butoxy-phenyl)-1-[(2,2-diethoxy-ethyl)-(1H-indazol-7-ylmethyl)-carbamoyl]-ethyl}-butyramide (3.46 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give the 6-(4-Hydroxy-benzyl)-8-(1H-indazol-7-ylmethyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (0.923 g, 3 step yield: 29%). ¹H NMR (CDCl₃, 300 MHz) δ 8.30 (s, 1H), 7.4-7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.85 (m, 3H), 6.8 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.2 (t, J=7.2, 2H) 1.45 (m, 3H) MS ESI 553 (M+H), 575 (M+Na).

Preparation Example 9 (1) Preparation of Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-amine

To a solution of Benzothiazole-4-carbaldehyde (1.96 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.74 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (16 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH 6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and Ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to give [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (5.32 g, 2 step Yield 70%). MS ESI 634 (M+H)

(3) Preparation of 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amide

To a solution of [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (3.64 g, 5.76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-N-benzothiazol-4-ylmethyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide which was used next step without further purification.

To a solution of 2-Amino-N-benzothiazol-4-ylmethyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide in CH₂Cl₂(50 mL) was added a solution of (3R)-3-(3-Benzyl-ureido)-hex-5-enoic acid (1.6 g, 6.1 mmol), EDCl (1.17 g, 1.2 eq), HOBt (0.93 g, 1.2 eq), DIEA (2.13 mL, 12.2 mL) in CH₂Cl₂ (100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 744 (M+H), 766 (M+Na)

(4) Preparation of 2-Allyl-8-benzothiazol-4-ylmethyl-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude 3-(3-Benzyl-ureido)-hex-5-enoic acid [1-[benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-amide (3.67 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give 2-Allyl-8-benzothiazol-4-ylmethyl-6-(4-hydroxy-benzyl)-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.2 g, 3 step yield: 35%). ¹H NMR (CDCl₃, 300 MHz) δ 9.20 (5, 1H), 7.4˜7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.80 (m, 3H), 6.75 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=1H), 5.05 (d, J=10.75, 1H), 5.0 (d, J=18.54, 1H), 4.87 (d, J=14.51, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.6-2.4 (m, 2H), 2.2 (t, J=7.2, 2H) MS ESI 596 (M+H), 618 (M+Na).

Preparation Example 10 (1) Preparation of Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-amine

To a solution of Benzothiazole-4-carbaldehyde (1.96 g, 12 mmol) in MeOH (50 mL) was added aminoacetaldehyde diethyl acetal (1.74 mL, 12 mmol) and acetic acid (1.03 mL, 18 mmol). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was added to a stirred solution of sodium cyanoborohydride (816 mg, 13 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was used next step without further purification.

(2) Preparation of [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester

To a solution of Cbz-Try(O^(t)Bu)-OH (6.63 g, 12 mmol) in MC/DMF (9/1, 100 mL) was added HATU (4.56 g), and DIEA (4.2 mL). The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was added to a stirred solution of Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-amine. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure. Then H₂O and ethyl acetate were added to the reaction mixture. The organic layer was washed with H₂O and brine, dried over Na₂SO₄, and concentrated under reduced pressure. The crude compound was purified by chromatography to gave [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (5.32 g, 2 step yield: 70%). MS ESI 634 (M+H)

(4) Preparation of N-[1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-3-(3-benzyl-ureido)-butyramide

To a solution of [1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)-ethyl]-carbamic acid benzyl ester (3.64 g, 5.76 mmol) in MeOH (50 mL) was added Pd/C (500 mg). After 2 h of stirring under H₂ atmosphere, the solution was filtered on Celite and the solvent was evaporated to afford 2-Amino-N-benzothiazol-4-ylmethyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide, which was used next step without further purification.

To a solution of 2-Amino-N-benzothiazol-4-ylmethyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide in CH₂Cl₂(50 mL) was added a solution of (3R)-3-(3-Benzyl-ureido)-butyric acid (1.44 g, 6.1 mmol), EDC (1.17 g, 7.32 mmol, 1.2 eq), HOBt (0.93 g, 7.32 mmol, 1.2 eq), DIEA (2.13 mL, 12.2 mmol, 2.4 eq) in CH₂Cl₂(100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 718 (M+H), 740 (M+Na).

(4) Preparation of 8-Benzothiazol-4-ylmethyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide

A solution of crude N-[1-[Benzothiazol-4-ylmethyl-(2,2-diethoxy-ethyl)-carbamoyl]-2-(4-tert-butoxy-phenyl)ethyl]-3-(3-benzyl-ureido)-butyramide (3.55 g, 4.95 mmol) in formic acid (100 mL) was stirred at room temperature for 13 h. The solvent was removed under reduced pressure and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The residue was purified by chromatography and recrystallized on ethyl acetate and hexane to give 8-Benzothiazol-4-ylmethyl-6-(4-hydroxy-benzyl)-2-methyl-4,7-dioxo-hexahydro-pyrazino[1,2-a]pyrimidine-1-carboxylic acid benzylamide (1.05 g, 3 step yield: 32%). ¹H NMR (CDCl₃, 300 MHz) δ 9.25 (s, 1H), 7.4˜7.26 (m, 3H), 7.2 (d, J=7.01, 2H), 6.98 (t, J=8.0, 1H), 6.85 (m, 3H), 6.8 (t, J=7.0, 1H), 6.5 (d, J=8.76, 2H), 5.6 (m, 1H), 5.25 (t, J=4.7, 1H), 4.55 (m, 1H), 4.5˜4.25 (m, 4H), 3.5˜3.3 (m, 2H), 3.25˜3.1 (m, 2H), 2.2 (t, J=7.2, 2H) 1.45 (m, 3H) MS ESI 570 (M+H), 592 (M+Na).

Example 1

(1) Preparation of N^(β)-Moc-N^(α)-benzyl-hydrazinoglycine

This compound was prepared according to literature procedure. (Cheguillaume et. al., Synlett 2000, 3, 331)

(2) Preparation of 1-Methoxycarbonyl-2,8-dibenzyl-6-methyl-4,7-dioxo-hexahydro-pyrazino[2,1-c][1,2,4]triazine

Bromoacetal resin (60 mg, 0.98 mmol/g) and a solution of benzyl amine in DMSO (2.5 ml, 2 M) were placed in vial with screw cap. The reaction mixture was shaken at 60° C. using rotating oven [Robbins Scientific] for 12 hours. The resin was collected by filtration, and washed with DMF, then DCM to provide a first component piece.

A solution of Fmoc-alanine (4 equiv., commercially available, the second component piece), HATU (PerSeptive Biosystems, 4 equiv.), and DEA (4 equiv.) in NMP (Advanced ChemTech) was added to the resin. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

To the resin was added 20% piperidine in DMF. After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

A solution of N^(β)-Moc-N^(α)-benzyl-hydrazinoglycine (4 equiv., compound (3) in preparative example 2, where R₇ is benzyl, 3^(rd) component piece), HOBT [Advanced ChemTech] (4 equiv.), and DIC (4 equiv.) in DMF was added to the resin prepared above. After the reaction mixture was shaken for 3 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then MeOH. The resin was dried in vacuo at room temperature.

The resin was treated with formic acid (2.5 ml) for 18 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under reduced pressure to give the product as an oil. ¹H-NMR (400 MHz, CDCl₃) δ ppm; 1.51 (d, 3H), 2.99 (m, 1H), 3.39 (d, 1H), 3.69 (m, 1H), 3.75 (m, 1H), 3.82 (5, 3H), 4.02 (d, 1H), 4.24 (d, 1H), 4.39 (d, 1H) 4.75 (d, 1H), 5.14 (q, 1H), 5.58 (dd, 1H), 7.10˜7.38 (m, 10H).

Example 2

(1) Preparation of N′-Fmoc-N-methyl-hydrazinocarbonyl chloride

An ice-cooled biphasic mixture of N-methyl hydrazine carboxylic acid 9H-fluoren-9-ylmethyl ester (107 mg, 0.4 mmol) in 15 ml of CH₂Cl₂ and 15 ml of saturated aq. NaHCO₃ was rapidly stirred while 1.93 M phosgene in toluene (1.03 ml, 2 mmol) was added as a single portion. The reaction mixture was stirred for 30 min, the organic phase was collected, and the aqueous phase was extracted with CH₂Cl₂. The combined organic layers were dried over MgSO₄, filtered, and concentrated in vacuo to afford 128 mg (97%) of carbamoyl chloride as a foamy solid. [Caution: Phosgene vapor is highly toxic. Use it in a hood]. This product was used for the following solid phase synthesis without further purification.

(2) Preparation of 2,5-Dimethyl-7-benzyl-3,6-dioxo-hexahydro-[1,2,4]triazolo[4,5-a]pyrazine-1-carboxylic acid benzylamide

Bromoacetal resin (30 mg, 0.98 mmol/g) and a solution of benzyl amine in DMSO (1.5 ml, 2 M) were placed in vial with screw cap. The reaction mixture was shaken at 60° C. using rotating oven [Robbins Scientific] for 12 hours. The resin was collected by filtration, and washed with DMF, then DCM, to provide the first component piece.

A solution of Fmoc-alanine (3 equiv., second component piece, commercially available), HATU (PerSeptive Biosystems, 3 equiv.), and DIEA (3 equiv.) in NMP (Advanced ChemTech) was added to the resin. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF, to thereby add the second component piece to the first component piece.

To the resin was added 20% piperidine in DMF. After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

A solution of N′-Fmoc-N-methyl-hydrazinocarbonyl chloride (combined third and fourth component pieces, 5 equiv.) obtained in the above step (1), DIEA (5 equiv.) in DCM was added to the resin prepared above. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and DMF.

To the resin was added 20% piperidine in DMF (10 ml for 1 g of the resin). After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

The resin was treated with a mixture of benzyl isocyanate (4 equiv.) and DIEA (4 equiv.) in DCM for 4 hours at room temperature. Then, the resin was collected by filtration and washed with DMF, DCM, and then MeOH. The resin was dried in vacuo at room temperature.

The resin was treated with formic acid for 14 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under reduced pressure to give the product as an oil.

¹H-NMR (400 MHz, CDCl₃) δ ppm; 1.48 (d, 3H), 2.98 (s, 3H), 3.18 (m, 1H), 3.46 (m, 1H), 4.37-4.74 (m, 5H), 5.66 (dd, 1H), 6.18 (m, 1H) 7.10-7.40 (m, 10H).

Example 3 Preparation of 2,5,7-Trimethyl-3,6-dioxo-hexahydro-[1,2,4]triazolo[4,5-a]pyrazine-1-carboxylic acid benzylamide

The title compound is prepared according to the same procedure as described in Example 2, but reacting bromoacetal resin with a solution of methyl amine instead of benzyl amine. ¹H-NMR (400 MHz, CDCl₃) δ ppm; 1.48 (d, 3H), 2.99 (s, 3H), 3.03 (s, 3H), 3.38 (m, 1H), 3.53 (dd, 1H), 4.36 (dd, 1H), 4.52 (q, 1H), 4.59 (dd, 1H), 5.72 (dd, 1H), 6.19 (br.t, 1H), 7.10-7.38 (m, 5H).

Example 4 Preparation of 2-Methyl-5-(p-hydroxyphenylmethyl)-7-naphthylmethyl-3,6-dioxo-hexahydro-[1,2,4]triazolo[4,5-a]pyrazine-1-carboxylic acid benzylamide

Bromoacetal resin (30 mg, 0.98 mmol/g) and a solution of naphthylmethyl amine in DMSO (1.5 ml, 2 M) were placed in vial with screw cap. The reaction mixture was shaken at 60° C. using rotating oven [Robbins Scientific] for 12 hours. The resin was collected by filtration, and washed with DMF, then DCM to provide the first component piece.

A solution of Fmoc-Tyr(OBut)-OH (3 equiv.), HATU (PerSeptive Biosystems, 3 equiv.), and DIEA (3 equiv.) in NMP (Advanced ChemTech) was added to the resin. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF, to thereby add the second component piece to the first component piece.

To the resin was added 20% piperidine in DMF. After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

A solution of N′-Fmoc-N-methyl-hydrazinocarbonyl chloride (5 equiv.), DIEA (5 equiv.) in DCM was added to the resin prepared above. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and DMF.

To the resin was added 20% piperidine in DMF (10 ml for 1 g of the resin). After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

The resin was treated with a mixture of benzyl isocyanate (4 equiv.) and DIEA (4 equiv.) in DCM for 4 hours at room temperature. Then, the resin was collected by filtration and washed with DMF, DCM, and then MeOH. The resin was dried in vacuo at room temperature.

The resin was treated with formic acid for 14 hours at room temperature. After the resin was removed by filtration, the filtrate was condensed under reduced pressure to give the product as an oil.

¹H-NMR (400 MHz, CDCl₃) δ ppm; 2.80-2.98 (m, 5H), 3.21-3.37 (m, 2H), 4.22-4.52 (m, 2H). 4.59 (t, 1H), 4.71 (d, 1H), 5.02 (dd, 1H), 5.35 (d, 1H), 5.51 (d. 1H), 6.66 (t, 2H), 6.94 (dd, 2H), 7.21-8.21 (m, 12H).

Example 5 Preparation of 2-Methyl-6-(p-hydroxyphenylmethyl)-8-naphthyl-4,7-dioxo-hexahydro-pyrazino[2,1-c][1,2,4]triazine-1-carboxylic acid benzylamide

Bromoacetal resin (60 mg, 0.98 mmol/g) and a solution of naphthyl amine in DMSO (2.5 ml, 2 M) were placed in vial with screw cap. The reaction mixture was shaken at 60° C. using rotating oven [Robbins Scientific] for 12 hours. The resin was collected by filtration, and washed with DMF, then DCM.

A solution of Fmoc-Tyr(OBut)-OH (4 equiv.), HATU [PerSeptive Biosystems] (4 equiv.), and DIEA (4 equiv.) in NMP (Advanced ChemTech) was added to the resin. After the reaction mixture was shaken for 4 hours at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

To the resin was added 20% piperidine in DMF. After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

A solution of N^(β)-Fmoc-N^(α)-benzyl-hyrazinoglycine (4 equiv.), HOBT [Advanced ChemTech] (4 equiv.), and DIC (4 equiv.) in DMF was added to the resin prepared above. After the reaction mixture was shaken for 3 hours at room temperature, the resin was collected by filtration and washed with DMF, and then DCM. To the resin was added 20% piperidine in DMF (10 ml for 1 g of the resin). After the reaction mixture was shaken for 8 min at room temperature, the resin was collected by filtration and washed with DMF, DCM, and then DMF.

The resin was treated with a mixture of benzyl isocyanate (4 equiv.) and DIEA (4 equiv.) in DCM for 4 hours at room temperature. Then, the resin was collected by filtration and washed with DMF, DCM, and then MeOH. After the resin was dried in vacuo at room temperature, the resin was treated with formic acid (2.5 ml) for 18 hours at room temperature. The resin was removed by filtration, and the filtrate was condensed under reduced pressure to give the product as an oil.

¹H-NMR (400 MHz, CDCl₃) δ ppm; 2.73 (s, 3H), 3.13 (d, 1H), 3.21-3.38 (m, 3H), 3.55 (d, 1H), 3.75 (t, 1H), 4.22 (dd, 1H), 4.36 (dd, 1H), 4.79 (d, 1H), 5.22 (t, 1H), 5.47 (m, 2H), 6.68 (d, 2H), 6.99 (d, 2H), 7.21-821 (m, 12H);

MS (m/z, ESI) 564.1 (MH⁺) 586.3 (MNa⁺).

Example 6 Bioassay for the Measurement of IC₅₀ against SW480 Cells and Cytotoxicity Test on the Cell Lines

The test compound (Compound A) used in this example was prepared in Example 4.

a. Reporter Gene Assay

SW480 cells were transfected with the usage of Superfect™ transfect reagent (Qiagen, 301307). Cells were trypsinized briefly 1 day before transfection and plated on 6 well plate (5×10⁵ cells/well) so that they were 50-80% confluent on the day of transfection.

Four microgram (TOPFlash) and one microgram (pRL-null) of DNAs were diluted in 150 μl of serum-free medium, and 30 μl of Superfect™ transfect reagent was added. The DNA-Superfect mixture was incubated at room temperature for 15 min, and then, 1 ml of 10% FBS DMEM was added to this complex for an additional 3 hours of incubation. While complexes were forming, cells were washed with PBS twice without antibiotics.

The DNA-Superfect™ transfect reagent complexes were applied to the cells before incubating at 37° C. at 5% CO₂ for 3 hours. After incubation, recovery medium with 10% FBS was added to bring the final volume to 1.18 ml. After 3 hours incubation, the cells were harvested and reseeded to 96 well plate (3×10⁴ cells/well). After overnight incubation at 37° C. at 5% CO₂, the cells were treated with Compound A for 24 hours. Finally, the activity was checked by means of luciferase assay (Promega, E1960).

FIG. 3 illustrates the results of the measurement of IC₅₀ of Compound A for SW480 cells.

b. Sulforhodamine B (SRB) Assay

Growth inhibitory effect of Compound A on the cells listed below measured by the sulforhodamine B assay. SW480 cells in 100 μl media were plated in each well of 96-well plate and allowed to attach for 24 hours. Compound A was added to the wells to produce the desired final concentrations, and the plates were incubated at 37° C. for 48 hours. The cells were then fixed by gentle addition of 100 μl of cold (4° C.) 10% trichloroacetic acid to each well, followed by incubation at 4° C. for 1 hour. Plates were washed with deionized water five times and allowed to air dry. The cells were then stained by addition of 100 μl SRB solution (0.4% SRB(w/v) in 1% acetic acid (v/v)) to wells for 15 min. After staining, the plates were quickly washed five times with 1% acetic acid to remove any unbound dye, and allowed to air dry. Bound dye was solubilized with 10 mmol/L Tris base (pH 10.5) prior to reading the plates. The optical density (OD) was read on a plate reader at a wavelength of 515 nm with Molecular Device. Inhibition of growth was expressed as relative viability (% of control) and GI₅₀ was calculated from concentration-response curves after log/probit transformation.

Table 6 shows in vitro cyclotoxicity (SRB) assay data for Compound A obtained in Example 4. The values in Table 6 are in μg/ml.

TABLE 6 Origin Cell Example 4 Cisplatin 5-FU Colon T84 1.134 >10 1.816 LOVO 0.532 >10 1.029 HT29 1.694 >10 5.334 DLD-1 1.775 >10 >10 COLO205 1.136 >10 1.130 CACO-2 1.201 >10 0.451 SW480-Kribb 1.137 >10 >10 SW480-CWP 0.980 4.502 >10 SW620 1.426 >10 5.570 KM12 1.451 >10 2.729 HCT15 2.042 >10 1.179 HCT116 0.96  >10 1.039 HCC2998 1.047 >10 5.486 786-0 1.417 3.347 0.584 Leukemia HL60 1.243 >10 7.010 RPMI8226 1.1.177 >10 >10 K562/VIN 1.640 >10 7.071 K562/ADR 7.682 >10 >10 K562 1.247 >10 6.133 Prostate PC3 1.207 >10 >10 HT1080 1.469 >10 0.798 Lung A549 1.386 >10 1.007 NCI H460 1.498 >10 1.397 NCI H23 1.296 5.176 2.254 Renal 293 0.731 6.641 2.015 CAKI-1 0.467 >10 0.925 ACHN 1.263 5.019 5.062 Melanoma RPMI7951 0.936 5.010 0.920 M14 2.289 3.447 1.225 HMV-II 4.834 3.190 0.695 HMV-I 1.153 5.478 2.110 G361 0.584 4.827 1.539 CRL1579 1.830 0.699 >10 A431 1.083 3.722 0.404 A253 1.398 2.084 2.926 UACC62 0.563 >10 1.093 SK-MEL-28 1.291 >10 >10 SK-MEL-5 0.888 >10 2.434 LOX-IMVI 1.526 >10 >10 A375 1.391 >10 1.464 Breast MCF7/ADR 9.487 9.907 >10 MCF7 7.355 >10 1.751

Example 7 Min Mouse Model

Selected compounds of the present invention (Compound B and Compound C) were evaluated in the min mouse model to evaluate their efficacy as anti-cancer agents.

The min mouse model is a widely used model to test for this type of efficacy. The numbers of polyp formed in small intestine and colon of these mice after various treatments were measured (Table 7). The data shown that both compounds, when administered at about 300 mpk, reduce the number of polyp in min mice compared to those in the control mice treated with vehicle only.

TABLE 7 MIN MOUSE MODEL DATA Polyp Number (Mean ± S.D.) P % In- Small (total) hibition Group Intestine Colon Total Vs. VH vs. VH Wild Type 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0 — — Vehicle 65.8 ± 15.9 1.8 ± 1.5 67.7 ± 15.3 — — Compound 69.2 ± 20.8 1.7 ± 1.5 71.4 ± 23.0 — — C - 100 mpk Compound 46.1 ± 17.1 1.1 ± 1.2 47.0 ± 16.9 <0.01 31 C - 300 mpk Compound 45.2 ± 22.1 1.4 ± 0.9 46.8 ± 17.0 <0.01 31 B - 300 mpk Sulindac - 48.0 ± 20.7 0.5 ± 0.5 48.5 ± 20.9 <0.05 28 160 ppm

Example 8 Chemogenomic Inhibition of CBP/β-Catenin Interaction Rescues Defects in Neuronal Differentiation Caused by a Presenilin-1 Mutation

The following compound (Compound D) used in this example:

Materials and Methods

Plasmids, TOPFLASH and FOPFLASH reporter constructs were transformed into DH5α competent cells by standard protocol. Plasmids used for transfection assays were isolated and purified using EndoFree Maxi Kit (Qiagen, Valencia, Calif.).

PC-12 Cell Culture. PC-12 cells were maintained in RPMI 1640 supplemented with 10% horse serum, 5% fetal bovine serum, 4.5 g/L glucose, 2 mM L-glutamine, 1.0 mM sodium pyruvate and 10 μg/ml penicillin-streptomycin.

Cell Differentiation. Cell culture dishes were pre-coated overnight with 0.25 mg/ml collagen (Cohesion, Calif.), 10 μg/ml Poly-L-Lysine (Sigma-Aldrich, St. Louis, Mo.) and 12 μg/ml Polyethyleneimine (ICN, La Mesa, Calif.). Cells were cultured on coated dishes at 15,000 cells/cm², and differentiated into a neuron-like phenotype by incubation in medium with reduced serum (1% fetal bovine serum), containing 50 ng/ml nerve growth factor (NGF) (Sigma-Aldrich) for 10 days. NGF-containing medium was changed every 2-3 days.

Treatment with Compound D. Compound D, a small molecule inhibitor of β-catenin/CBP interaction, was dissolved in DMSO at a stock concentration of 100 mM. Differentiated PC-12/L286V cells were treated with increasing concentrations of this compound for 4 hours. Transfection was then initiated after this treatment period. For cell differentiation experiments, Compound D was added at a concentration of 10 μM, together with NGF, for the entire differentiation period.

Transfection. PC-12 cells were cultured and differentiated on 60-mm dishes. At the end of the 10-day differentiation period, cells were transfected with 2 μg reporter constructs, TOPFLASH and FOPFLASH, per 60-mm dish. Transfections were performed using Superfect (Qiagen) according to manufacturer's instructions.

Luciferase Assays. Cells were lysed, 6 hours after transfections, in 100 μl of Cell Culture Lysis Reagent (Promega, Madison, Wis.), and scraped into microcentrifuge tubes. Tubes were then centrifuged briefly (about 10 seconds) at 12000 rpm to pellet cell debris. Luciferase activity was measured on 20 μl of cell lysate and 100 μl substrate from the Luciferase Assay System (Promega). Luciferase activity was measure using Packard LumiCount. (Hewlett Packard). Quantitation of luciferase was performed in triplicates, and repeated in at least three independent experiments.

Immunofluorescence. Cells were plated at a density of 10,000 cells/cm² on sterile coated 22×22 mm coverslips in a 6-well culture plate. Differentiation was initiated, as previously described, for 10 days. The differentiated cells were then fixed in methanol for 15 minutes at −20° C. This is followed by a 15 minutes incubation with PBS+0.1% Triton X-100. The coverslips were incubated with antibodies raised against Ephrin B2 Receptor (Santa Cruz Biotechnology) and Gap-43 (Novus Biologicals) for 40 minutes at 37° C. After a series of washes with PBS-Triton X-100, secondary antibody conjugated to FITC (Jackson ImmunoResearch, Westgrove, Pa.) was applied. All slides images were acquired using a Nikon PCM2000 Laser Scanning Confocal Microscope mounted on a Nikon Eclipse E600 upright microscope (Nikon, Melville, N.Y.).

Quantitation of Neurite Outgrowth. Cell counts were taken from six randomly chosen microscopic fields (10×). In each field, total number of cells, as well as cells that displayed neurites greater than twice the length of the cell body was determined. The number of cells with such outgrowths was then expressed as a percentage of the total number of cells. Values obtained were from duplicates of three independent experiments.

RT-PCR. To analyze the mRNA levels for Ephrin B2 (EphB2) receptor, total RNA was isolated using Trizol (Invitrogen-GIBCO-BRL, Baltimore, Md.) from differentiated cells. 2 μg RNA was reverse transcribed in a total volume of 20 μl with random hexamer (50 ng), and using the Superscript II reverse transcription system (Invitrogen-GIBCO-BRL), according to manufacturer's guidelines. PCR was carried out in a 50 μl volume containing 5 μl cDNA, 100 pmol primers, 100 μM dNTPs, 1×Taq buffer and 1.5 mM MgCl₂. Reaction mixtures were heated to 80° C. for 10 min, after which Taq was added. cDNAs were amplified for 25 (EphB2 receptor) or 15 (GAPDH) cycles. One round of amplification consisted of 1 min at 94° C., 2 min at 60° C., and 2 min at 72° C., with a final extension time of 10 min at 72° C. The PCR products were resolved and visualized by electrophoresis in a 2% gel, stained with ethidium bromide. EphB2 receptor PCR primers used were, 5′-CACTACTGGACCGCACGATAC-3′ and 5′-TCTACCGACTGGATCTGGTTCA-3′, Primer pairs for GAPDH were 5′-GGTGCTGAGTATGTCGTGGA-3′ and 5′ ACAGTGTTCTGGGTGGCAGT

Results

Rat PC-12 cells are derived from the neural crest lineage and upon nerve growth factor (NGF) treatment, undergo differentiation to a neurite-bearing sympathetic-like neuron (Greene and Tischler, Proc Natl Aced Sci USA 73, 2424 (1976)). Utilizing a PC-12 cell based model, the effects of an early-onset FAD associated PS-1 mutation, PS-1/L286V, on TCF/β-catenin mediated transcription and neuronal differentiation were characterized. It has been demonstrated that specifically blocking transcription mediated by TCF/β-catenin/CBP alleviates PS-1 induced defects in neuronal differentiation.

PC-12 cells stably overexpressing either wild type PS-1 (PS-1/WT) or mutant PS-1 (PS-1/L286V) and a vector-transfected control cell line (Guo et al., Neuroreport, 8, 379 (1996)) were plated on dishes coated with collagen, poly-L-lysine and poly-etheleneimine. Differentiation was induced by treatment with 50 ng/ml of NGF for 10 days. Overexpressing PS-1/WT cells or the vector-transfected cells had extensive neurite formation (similar to PC-12 cell clones from ATCC), whereas the PS-1/L286V mutant cells had only stubby neurite formation (FIG. 4 A-C). Additionally, vector-transfected PC-12 control and PS-1/WT cells displayed extensive expression of the neuronal differentiation marker GAP-43 (Gorgels et al., Neurosci Lett 83, 59 (1987)) (FIG. 4 D,E), whereas the PS-1/L286V cells were essentially devoid of this marker (FIG. 4 F).

To assess the effects of the PS-1/L286V mutation on canonical Wnt/β-catenin signaling, we transiently transfected NGF treated PC-12 cells with Topflash, a Wnt/β-catenin signaling reporter construct (Morin et al., Science 275, 1787 (1997)). As seen in FIG. 4F, the overexpressing PS-1/WT cells had similar levels of TCF/β-catenin signaling compared to the vector control cells. However, the PS-1/L286V mutant cells displayed significantly (10-fold) increased Topflash expression. In contrast, the negative control reporter construct Topflash did not show any significant differences.

It was hypothesized that dysregulated TCF/β-catenin signaling in the PS-1/L286V mutant cells was responsible for the defective differentiation and neurite outgrowth. To test this hypothesis, a specific small molecule inhibitor of TCF/β-catenin signaling, Compound D (Emami et al., Cancer Cell, in press), was used. This small molecule selectively blocks the β-catenin/CBP interaction, but not the β-catenin/p300 interaction, thereby interrupting a subset of TCF/β-catenin transcription. Treatment of the PS-1/L286V mutant cells with 10 μM Compound D plus NGF decreased TCF/β-catenin reporter gene transcription, and led to essentially normal neurite outgrowth and differentiation (FIG. 5 A), similar to that seen in the overexpressing PS-1/WT cells (FIGS. 5 A, B), as compared to the untreated cells (FIG. 4 C). Furthermore, PS-1/L286V mutants treated with Compound D showed similar intense GAP-43 staining to the PS-1/WT and vector-transfected cells (FIG. 4 B). To demonstrate that Compound D treated mutant cells develop neurites similar to that of the vector control or PS-1/WT cells, cells that had neurites greater than twice the length of the cell body were counted. Treatment with Compound D substantially increased the percentage of cells bearing neurites to levels similar to that of the vector-transfected and overexpressing PS-1/WT cells (FIG. 5 C). It is concluded that blocking transcription mediated by TCF/β-catenin/CBP corrects many of the phenotypic defects in neurite outgrowth and neuronal differentiation due to the PS-1/L286V mutation.

Ephrin B2 receptors (EphB2) have been implicated in synapse formation (Wilkinson, Nat. Rev. Neurosci. 2, 155 (2001)) and the Ephrin A family has recently been shown to play a role in hippocampal dendritic spine morphology (Murai et al., Nat. Neurosci. 6, 153 (2003)). Focused EphB2 expression was observed, which localized with neuronal processes in the vector and PS-1/WT-transfected cells (FIG. 6 A, B), whereas the PS-1/L286V mutant cells demonstrated very weak and diffuse EphB2 signal (FIG. 6 C). Increased TCF/β-catenin signaling in PS-1/L286V mutant cells manifested itself in decreased EphB2 expression as judged by RT-PCR (FIG. 6 E, lane 3). Furthermore, addition of 10 μM Compound D led to increased EphB2 message (FIG. 6 E, lane 4) as well as EphB2 expression in these cells (FIG. 6 D). These results are consistent with the data of Bathe and colleagues (Bathe et al., Cell 111, 251 (2002)) who recently showed that expression of EphB2/EphB3 receptors and their ligand ephrin-B1 is inversely controlled in colonic crypts via TCF/β-catenin transcription, and that proper regulation is important for appropriate cell proliferation, differentiation and sorting. We present evidence that the PS-1/L286V mutation via increased TCF/β-catenin signaling, decreased the expression of EphB2 receptors and this is corrected by Compound D mediated inhibition of the β-catenin/CBP interaction.

Example 9 Compound D Causes a G1S-Phase Arrest and Activates Caspase Activity

Flow Cytometric Analysis (FACS)

For FACS analysis, approx. 5×10⁶ cells from Compound O-treated or vehicle-treated were fixed with 70% chilled ethanol and stored at −20° C. for at least 30 minutes. The cells were washed once with 1×PBS and incubated with propidium iodine (PI) solution (85 μg/ml propidium iodine, 0.1% Nonidet P-40, 10 mg/ml RNAse) for 30 minutes at room temperature. 10,000 stained cells for each sample were acquired using Beckman Coulter EPICS XL-MCL Flow Cytometry and the percentage of cells in different phase of the cell cycle was determined by Expo32 ADC software (Coulter Corporation, Miami, Fla., 33196).

Caspase-3 Activity Assay

SW480, HCT116, and CCD18Co cells were plated at 10⁵ cells per well (96-well plates) for 24 hours prior to treatment. 25 μM of Compound D or control (0.5% DMSO) was added to each well 24 hours post treatment, cells were lysed and caspase activity was measured using a caspase-3/7 activity kit (Apo-One Homogeneous caspase-317 assay, #G77905, Promega). Relative fluorescence units (RFU) were obtained by subtracting the unit values of the blank (control, without cells) from the experimental measured values.

Compound D Causes a G₁/S-Phase Arrest and Activates Caspase Activity

It has been shown that inhibition of the expression of the cyclin D1 gene causes arrest at the G₁/S-phase of the cell cycle (Shintani et al., “Infrequent alternations of RB pathway (Rb-p16INK4A-cyclin D1) in adenoid cystic carcinoma of salivary glands,” Anticancer Res. 20:2169-75 (2000)). HCT116 (FIG. 7A, upper panel) and SW480 (FIG. 7A, lower panel) cells were treated with Compound D (25 μM) (FIG. 7A, right) or control (0.5% DMSO) (FIG. 7A, left) for 24 hours. The cells were subsequently stained with propidium iodide (PI) and analyzed for DNA content by FACS cytofluorometry. As expected, the control cells, (FIG. 7A, left), were cycling normally whereas the Compound D treated cells (FIG. 7A, right) showed increased accumulation at G₁S-phase of the cell cycle. Thus, it can be seen that Compound D causes arrest of cells at the G₁ phase.

Caspases are cysteine proteases that are generally activated in a given population of cells triggered by apoptotic stimuli. To assess apoptotic induction in SW480, HCT116, and wild-type colonocytes (CCD18Co cells), the cells were treated with either Compound D (25 μM) or control (0.5% DMSO) for 24 hours, followed by an assay for caspase-3/7 activity. As shown in FIG. 7B, Compound D specifically and significantly activated the caspase-3/7 pathway in SW480 and HCT116 cells compared to CCD18Co cells.

Example 10 Compound D Reduces Proliferation of Transformed Colorectal Cells

Soft Agar Assays

The soft agar colony formation assay was conducted with SW480 cells by some modification of the procedure previously described (Moody et al., “A vasoactive intestinal peptide antagonist inhibits non-small cell lung cancer growth,” Proc. Natl. Acad. Sci. USA. 90:4345-49 (1993)).

Each well (35 mm) of a 6-well plate (Nalge Nunc International, Roskide, Denmark) was coated with 1 ml of 0.8% bottom agar in DMEM medium containing 10% fetal bovine serum. After it was solidified, 1 ml of DMEM medium containing 0.4% top agar, 10% fetal bovine serum, compound doubly concentrated, and 5,000 single viable cells was added to each well. The cultures were incubated at 37° C. in humidified 5% CO₂ incubator. Colonies in soft agar were monitored daily and photographed after incubation for 8 days. Colonies 60 μm in diameter were counted.

Compound D Reduces Proliferation of Transformed Colorectal Cells

Soft agar colony forming assays were performed using SW480 cells treated with Compound D (0.25-5 μM) and 5-fluorouracil (5-FU) (0.5-32 μM). As shown in FIG. 8A, Compound D shows a dose dependent decrease in the number of colonies formed. IC₅₀ value of Compound D and 5-FU was 0.87±0.11 μM and 1.98±0.17 μM, respectively. Thus, Compound D increased caspase activity and reduced growth in vitro of colorectal cells that are transformed by mutations that activate β-catenin signaling.

Example 11 Compound C Reduces Tumor Growth in Nude Mouse Model

SW620 cells (9×10⁶ cells/mouse) were grafted into nude mice subcutaneously on Day 0. Mice received 200 mg/kg of Compound C intraperitoneally every other day until Day 21 after 4 times of 300 mg/kg every other day starting Day 1. Compound C reduces the tumor growth in the treated mice compared to the vehicle control mice (FIG. 9A), and slightly reduces body weights of the treated mice compared to those of the vehicle control mice (FIG. 9B).

Example 12 Compound D Suprresses Survivin Expression

The effect of Compound D on survivin expression was studied at both transcriptional and translational levels. The methods used at the transcriptional level include cDNA microarray analysis, RT-PCR, survivin reporter assays and chromotin immunoprecipitation (ChIP). The methods used at translational levels include Western blot analysis and immunochemistry.

A plasmid containing luciferase under the control of survivin promoter was constructed and transfected into wild type, CBP+/−, or p300+/−3T3 cells. The results (FIG. 10) show that Wnt 1 stimulates expression of the survivin gene in all three types of cells, whereas Compound D reduces expression of the survivin gene and decreases the stimulation of the survinin gene expression by Wnt1 in those cells. Similarly, Compound D and its analog (Compound A) were shown to inhibit expression of survivin in SW480 cells (FIG. 11).

Real time reverse transcription-PCR analysis was performed according to the protocol provided with the SYBR Green PCR Master Mix Kit (Perkin Elmer Biosystems, Shelton, ST). Total RNA templates for the RT-PCR reactions were extracted with the RNeasy Midi Kit (Qiagen) from cells treated with Compound D (25 μM) or control (0.5% DMSO) 24 hours after treatment. The primers used for the RT-PCR reactions were 5′-AGCCCTTTCTCAAGGACCAC-3′ and 5′-GCACTTTCTTCGCAGTTTCC-3′. Table 8 shows the results of the analysis. A ratio less than 0.5 indicates a significant decrease of gene expression due to the treatment of Compound D, whereas a ratio greater than 1.5 indicates a significant increase of gene expression. A ratio about 1 indicates no change. As indicated in Table 8 and FIG. 12, the expression of the survivin gene is significantly reduced in the presence of Compound D compared to the control.

TABLE 8 Gene Expression with and without Compound D Ratio (Treated/ Gene DMSO Control) Ubiquitin 0.98 GADPH 0.98 HLAC 1.01 Survivin 0.30 PCNA 0.33 Antigen KI-67 0.45 MIC-1 7.0 GADD-153 7.00

ChIP assays on SW 480 cells treated with either Compound D (25 μM) or control (0.5% DMSO) were performed. As shown in FIG. 13, the survivin promoter is occurred by CBP, β-catenin, Tcf4 and acetylated histone in control treated cells. Treatment with Compound D decreases the association of all these proteins with the survivin promoter.

To characterize the effect of Compound D on the survivin expression at the translational level, Western blot analysis of extracts of cells treated with vehicle (0.5% DMSO) alone, 10 μM or 25 μM Compound D, or 5 μM 5-FU was performed using survivin 6E4 monoclonal antibody (Cell Signaling Technology). The results (FIG. 14A) show that the treatments with Compound D at both concentrations and the treatment with 5-FU reduced the amount of the survivin protein. The treatments with Compound D at both concentrations were more effective in reducing the survivin expression than the treatment with 5-FU, and the treatment with Compound D at the higher concentration (i.e., 25 μM) was most effective.

The effect of Compound D on the survivin expression at the translational level was further characterized using immunofluorescence microscopy. In the absence of Compound D, survivin localizes to the mitotic spindle apparatus, consistent with the notion that survivin is involved in chromosomal separation (FIG. 14B). This expression pattern was not observed in SW480 cells after the treatment of Compound D as little or no survivin protein was detected (FIG. 14C).

Example 13 Effects of Various Compounds on Survivin and TCF4 Expression

The effects of various compounds having general formula (I) on survivin and TCF4 expression were characterized. The results are shown in Table 9.

TABLE 9 Effects of compounds on survivin and TGF4 expression Survivin % inhibition TCF4 IC50 5 uM 25 uM (uM)

100 99 ~2

97 100 ~2.2

51 93 ~6.3

41 92 5.2 ± 0.7

0 6 18.2 ± 2.4 

0 80 1.3 ± 0.1

0 93 2.2 ± 0.2

46 96 4.4 ± 0.6

0 77 3.5 ± 0.3

0 92 7.3 ± 0.6

79 81 1.7 ± 0.2

0 84 4.8 ± 0.4

0 68 10.9 ± 1.3 

8 4 NA

9 91 1.4 ± 0.2

5 91  6.3 ± 0.431

0 94 2.6 ± 0.4

0 21 7.3 ± 1.1

0 91 5.2 ± 1.1

45 88 13.2 ± 4.1 

9 92 5.9 ± 0.5

6 58 11.2 ± 1.5 

48 96  3.9 ± 0.55

0 32 50.4 ± 7.0 

86 91 2.6 ± 0.6

27 98 10.7 ± 1.7 

80 97 4.6 ± 0.7

82 97 2.8 ± 0.4

6 89 13.9 ± 2.3 

14 99 10.7 ± 1.9 

25 44 27.1 ± 4.6 

Example 14 Compound D Promotes Apoptosis Via Suppression Of Survivin Expression

To determine the effect of Compound D on apoptosis and the role of survivin in such an effect, the activities of caspases 2 and 3 in cultured tumor cells treated with either Compound D or control were measured. The results (FIG. 15) show that (1) Compound D (at 2.5 μM or 5.0 μM) activated the caspase 3 activity, but not the caspase 2 activity; (2) stausporine (0.5 μM) increased both the caspase 2 and caspase 3 activities; (3) the co-treatment of stausporine and Compound D produced a synergic stimulation of the caspase 3 activity, but not a synergic stimulation of the caspase 2 activity; and (4) transfection of the survivin gene decreased the activation of the caspase 3 activity induced by the treatment of stausporine or Compound D, and the synergic stimulation of the caspase 3 activity induced by the co-treatment of stausporine and Compound D. The above results suggest that Compound D stimulate the caspase 3 activity via suppression of the expression of the survivin gene.

The effect of compound D on apoptosis and the role of survivin in such an effect were further characterized by measuring cell death of cultured tumor cells treated with staurosporine (0.5 μM), Compound D (5.0 μM) or both. The results (FIG. 16) showed that both Compound D and stausporine promote cell death, and that transfection of the survivin gene decreased the increase in cell death induced by the treatment of stausporine, Compound D, or both. The above results suggest that Compound D promote apoptosis via suppression of the expression of the survivin gene.

To determine the effect of Compound D on cell cycle and the role of survivin in such an effect, FACS analysis was performed on cultured tumor cells with or without transfection of a construct containing the survivin gene and further treated with stausporine (0.5 μM), Compound D (5 μM), or both. The results (FIG. 17) show that both stausporine and Compound D increase the number of cells in G₀, and that overexpression of survivin in the cells decreases the effect of the treatment of stausporine, Compound D, or both. These results suggest that the effect of Compound D on cell cycle may be at least partially via suppression of the expression of the survivin gene.

Example 15 Preparation and Activity of Prodrugs

(1) General Procedure for Preparing Prodrugs by Phosphorylation of Phenol Group

The starting phenol (26.06 mmol) was dissolved in tetrahydrofuran (130 ml), followed by addition of triethylamine (TEA) (10.9 ml, 78.18 mmol) at room temperature. The reaction mixture was cooled to 5° C., and then POCl₃ (12.2 ml, 130.3 mmol) was added slowly. After addition was finished, the mixture was allowed to warm to room temperature, and stirred at this temperature for 5 hours. After the reaction was completed, the mixture was poured into celite-pad filter funnel to remove TEA-HCl salt. Organics was diluted with water (130 ml) at 5° C., followed by adjusting pH 7˜8 using sodium bicarbonate (50 g), and the resulting basic solution was stirred overnight at room temperature. The resulting aqueous layer was washed with EtOAc (100 ml), and then lyophilized. The crude product was dissolved in methylene chloride (100 ml), followed by for 1 hour at room temperature. Inorganic salts were removed by filtration using celite pad, then solvent was evaporated. The crude product was purified by recrystallization (EA/Ether) to get 9.5 g of phosphorylated product as an off-white solid.

(2) Typical Work-Up Procedure for the Free Form of Phosphate

After washing the resulting basic aqueous layer, the solution was acidified to pH 3˜4 using 1N HCl, and then the phosphate free form was extracted twice with chloroform (300 ml). The organic layer was dried over sodium sulfate, and the crude product was purified by recrystallization.

(3) Converting Method from Free Form to Di-Sodium Form

A. Titration method

Free form of phosphate can be transformed to di-sodium salt form by titration, which could use many inorganic bases. For example, sodium carbonate, sodium bicarbonate, and sodium hydroxide are used in this experiment to produce di-sodium form. Other cations can be used to make different di-salt forms.

1. Analytical method and instrument for titration

-   -   a. Instrument: TitraLab (RADIOMETER COPENHAGEN)     -   Electrode: pHG201 pH glass electrode (RADIOMETER COPENHAGEN,         945-462)     -   REF201 reference electrode with KCl salt-bridge solution         (RADIOMETER COPENHAGEN, 945-463)     -   Titrant: 10 M Na, CO₃     -   Burette speed (titration speed): 15% (=1.5 ml/min)     -   Sample: 50 mg dissolved in distilled water (30 ml)     -   b. Results     -   pH 4 (start pH=2)

EP1 EP2 n start pH pH Titrant (ml) pH Titrant (ml) 1 2.10 4.21 9.50 8.15 19.03 2 2.08 4.26 10.28 8.02 19.12 Mean 2.09 4.24 9.89 8.09 19.08 B. Using Organic Sodium Donor

The basic drawback of titration using inorganic base is that the water must be used for the solvent. So searching the sodium donor dissolved freely in normal organic solvent is the easiest way to solve the problem. Several reagents such as sodium acetate and sodium ethylhexanoic acid were tested and found to be useful for making a di-sodium salt form.

Table 10 shows compounds for bioactivity test selected from the prodrugs of the present invention and IC₅₀ values thereof, which are measured by the reporter gene assay (RGA) and oncogenic activity by MTS or Sulforhodamine B assay as described in Example 6. The compound numbers on Table 10 are unrelated to those in Table 4 or 5.

TABLE 10 THE REPORTER GENE ASSAY AND ONOOGENIC ACTIVITY BY MTS OR SULFORHODAMINE B ASSAY FOR SELECTED PRODRUG COMPOUNDS Assay RGA, RGA, TopF Survivin MTS, SW480 MTS, HCT116 IC50, IC50, (uM) (uM) No Structure uM uM LD50 GI50 LD50 GI50 1

4.2 6.4 17.0 2.0 16.1 2.2 2

3.5 5.7 8.2 3.1 23.2 6.6 3

11.5 ND up to 50 uM 3.0 41.9 3.1 4

7.3 6.5 ND up to 50 uM 6.9 49.3 11.4 5

26.0 34.0 5.2 ND up to 50 uM 16.5 6

0.8 0.1 9.2 0.5 6.4 0.4 7

2.3 1.0 12.9 2.2 12.0 1.8 8

1.4 0.9 21.6 2.1 23.2 1.9 9

9.6 6.0 ND up to 50 uM 7.6 ND up to 50 uM 14.7 10

2.8 1.7 9.4 0.9 7.9 0.8 11

10.3 6.7 ND up to 50 uM 6.5 ND up to 50 uM 6.3 12

1.0 0.7 ND up to 50 uM 1.0 19.3 1.2 13

1.8 0.9 21.1 2.3 20.0 1.7 14

1.7 1.2 21.1 2.3 16.0 2.1

Example 16 Solubility of Selected Prodrugs

General Procedure for Solubility Test of Prodrugs

About 2 mg of each prodrug was dissolved in 1 ml of JP1 or JP2 solution as indicated below. Incubating at a temperature of 37° C., 200 ul of samples were withdrawn at 0 hour, 2 hour and 20 hour. Withdrawn samples were filtered through 0.45 μm syringe filters and analyzed by HPLC system.

Composition of Artificial Gastro-Intestinal Fluids (JP1, JP2)

JP1 JP2 PH 1.2 pH 6.8 NaCl 2.0 g 0.2 M KH₂PO₄ 250 ml 10% HCl 24.0 ml 0.2N NaOH 118 ml Distilled H₂O Adjusted to 1 L Distilled H₂O Adjusted to 1 L

Table 11 below shows the results of solubility test of selected prodrugs. The compound numbers on Table 11 are unrelated to those in Table 4, 5 or 10.

TABLE 11 AQUEOUS SOLUBILITY FOR SELECTED PRODRUG COMPOUNDS Solubility (37° C., ug/mL) 0 hr, 2 hr, 20 hr No Structure JP1 (pH l.2) JP2 (pH 6.8) 1

60.1 87.3 92.8 1797 1867 1894 2

122 173 160 1950 1939 1940 3

1878 1971 2036 1325 1902 2005 4

554 646 756 1982 2014 2030 5

406 532 684 1761 1778 1758 6

1453 1724 1787 1829 1864 1867 7

309 446 521 2145 2221 2239 8

671 775 921 2295 2317 2272 9

2251 2275 2403 2322 2353 2421 10

2292 2274 2327 2028 2055 2027 11

2006 2000 1998 1636 1654 1651

Example 17 Preparation of Dimethyl-carbamic acid 4-[2-allyl-1benzylcarbamoyl-8-(2,4-difluoro-benzyl)-4,7-dioxo-octahydro-pyrazino[2,1-c][1,2,4]triazin-6-ylmethyl]-phenyl ester

To a stirred solution of starting material (SM) (8.0 g, 13.9 mmol) and potassium carbonate (5.8 g, 41.7 mmol) in dimethylformamide was added dimethylcarbamyl chloride (3.0 g, 27.8 mmol). The reaction mixture was stirred overnight and then dissolved in EtOAc, washed with water five times. The combined organic layer was washed with brine, dried over sodium sulfate, concentrated in vacuo. The residue was chromatographed on silica gel with neat EtOAc to afford product (4.2 g, 32%). The data from analyzing the resulting product by mass spectrometry and NMR are:

MS (ESI) m/e 647 (M+1), 669 (M+Na).

¹H-NMR (300 MHz, CDCl₃) δ 7.27-7.39 (6H, m), 6.78-7.13 (6H) 6.68 (1H, t, J=6.0 Hz), 5.61-5.70 (2H, m), 5.34 (1H, t, J=6.0 Hz), 5.06-5.20 (2H, m), 4.31-4.69 (4H, m), 3.24-3.58 (8H, m), 3.07 (3H, s), and 2.99 (3H, s).

Example 18 Preparation of Carbonic acid 4-[2-allyl-1-benzylcarbamoyl-8-(2,4-difluoro-benzyl)-4,7-dioxo-octahydro-pyrazino[2,1-c][1,2,4]triazin-6-ylmethyl]phenyl ester 4-nitro-phenyl ester (2)

To a stirred solution of 2-Allyl-8-(2,4-difluoro-benzyl)-6-(4-hydroxy-benzyl)-4,7-dioxohexahydro-pyrazino[2,1-c][1,2,4]triazine-1-carboxylic acid benzylamine (1) (2 g, 3.47 mmol) in THF (40 ml) was added Triethylamine(0.97 ml, 6.95 mmol) and 4-nitrophenylchloroformate (0.7 g, 3.47 mmol). After stirring at room temperature for overnight, the solvent was removed under reduced pressure. The crude compound was purified by chromatography (Hexane, EtOAc 1:1) to give the compound (1.59 g, 62%). The data from analyzing the purified compound by TLC system and NMR are:

TLC System: R_(f)=0.3 (n-Hexane:EtOAc 1:1)

¹H NMR (300 MHz, CDCl₃). δ 3.25-3.60 (m, 8H), 4.35 (dd, J=14.9 Hz, 5.7 Hz, 1H), 4.43 (dd, J=14.8 Hz, 6.1 Hz, 1H), 4.52 (d, 14.5 Hz, 1H), 4.68 (d, 14.1H), 5.10 (d, 17.1 Hz, 1H), 5.21 (d, 10.3 Hz, 1H), 5.34 (t, J=6.1 Hz, 1H), 5.58 (dd, J=11.1 Hz 4.1 Hz, 1H), 5.67 (m, 1H), 6.71 (t, J=6.1 Hz, NH), 6.75-6.98 (m, 2H), 7.13 (d, J=8.4 Hz, 2H), 7.21 (d, J=8.7 Hz, 2H), 7.23-7.39 (m, 6H), 7.46 (d, J=9.5 Hz, 2H), and 8.30 (d, J=9.5 Hz, 2H).

Example 19 Preparation of (2-dimethylamino-ethyl)-carbamic acid 4-[2-allyl-1-benzylcarbamoyl-8-(2,4-difluoro-benzyl)-4,7-dioxo-octahydro-pyrazine[2,1-c][1,2,4]triazine-6-ylmethyl]-phenyl ester hydrochloride salt (3)

To a stirred solution of carbonic acid 4-[2-allyl-1-benzylcarbamoyl-8-(2,4-difluoro-benzyl)-4,7-dioxo-octahydro-pyrazino[2,1-c][1,2,4]triazin-6-ylmethyl]-phenyl ester 4-nitro-phenyl ester (2) (1.2 g, 1.62 mmol) in DMF (25 ml) was added N,N-Dimethylethylenediamine (0.26 ml, 2.43 mmol). After stirring at room temperature for overnight, the solvent was removed under reduced pressure. The residue was diluted with EtOAc and washed with water, brine. The organic layer was dried with Na₂SO₄ and concentrated in vacuo. The crude compound was purified by chromatography (n-Hexane:EtOAc, 1:1; EtOAc; CH₂Cl₂: MeOH, 9:1). The compound was poured with water and was maintained pH 5-6 with 1N eq. HCl to make HCl salt and then lyophilized to get the compound (0.75 g, 60%). The data from analyzing the resulting compound by TLC system and NMR are:

TLC System: R_(f)=0.35 (CH₂Cl₂:MeOH, 9:1)

ESI-MS: M+H⁺ 690.39

¹H NMR (300 MHz, CDCl₃): δ 2.56 (d, J=4.6 Hz, 6H), 3.18 (bm, 4H), 3.41-3.58 (m, 4H), 3.75 (t, J=10.3 Hz, 1H), 4.21 (bt, 2H), 4.35 (d, J=14.9 Hz 1H) 4.70 (d, J=14.9 Hz 1H), 5.05 (m, 1H), 5.12 (m, 1H), 5.42 (m, 6H), 5.80 (m, 1H), 6.91 (d, J=7.6 Hz, 2H), 7.04 (d, J=7.3, 2H), 7.09 (m, 1H), 7.18-7.26 (m, 6H), 7.31 (d, J=6.9 Hz, 2H), 7.33 (m, 1H), 7.84 (bt, NH), 7.98 (bt, NH), 10.7 (bs, 1H)

Example 20 Mouse In Vivo PK Study of Prodrug a after Single i.v. Bolus Injection

Animal Experiment

Drugs were prepared 10 mg/kg/5 ml in 10% Tween 80. Studies were performed in ICR mice. After i.v. bolus injection through the tail vein, blood samples were acquired from inferior vena cava at several time points and separated to plasma by centrifugation. Plasma samples were preserved at −20° C. until they were analyzed. Bleeding time points were 3, 6, 9, 17, 34, 67, 134, 202, 302 min. N=4.

Sample Preparation

For calibration curve, 98 ul aliquots of control mouse plasma were added 2 ul of drug stock solution and added 2 ul internal standard stock solution, 5 ug/ml of internal standard. Final concentrations of calibration samples were 1, 10, 100, 1000 ng/ml and 10 ug/ml. For plasma sample from animal experiment, 100 ul of plasma were added 2 ul of internal standard. Then, all the samples were added 500 ul of acetonitrile, 500 μl of ethylacetate and 100 ul of DW. Samples were mixed for 10 min and centrifuged. The supernatants were transferred another tubes and evaporated. Adding 200 ul of 40% acetonitrile, they were reconstituted and analyzed by LC-MS system.

Results

The changes of concentrations of prodrug A and its parent compound in mouse plasma with the increase of time after i.v. bolus injection of prodrug A are shown in FIG. 18. Square: parent compound; Diamond: prodrug A.

Example 21 Inhibitory Effects of Various Compounds on SW480 or HCT116 Cell Growth

SW480 or HCT116 cells were placed into 96 well microplate (10⁴ cells/well) and incubated for 24 hours at 37° C. 20 μl of [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt](MTS) solution (Promega) was added into each well and the absorbance after 2 hour incubation at 37° C. (negative control) was read. And then, the cells were treated with a test compound at various concentrations for 48 hours. 20 μl of MTS solution (Promega) was added into each well and incubated for 2 hour at 37° C. Cell viability was measured by reading the absorbance at 490 nm using a microplate reader (Molecular device) and cytotoxicity of a compound at each concentration was calculated. The results are shown in the table below.

Growth Inhibition GI50, uM) Structure SW480 HCT116

4.1 4.91

2.0 2.3

1.2 1.4

Example 22 Synergy of Compound A and 5-FU in Soft Agar Assay

Soft agar plates were prepared to contain 10% fetal bovine serum (FBS), 2 mM L-glutamine, 0.1 mM non-essential amino acid, 1× pen/strep (10000 units/mL Penicillin, 10000 ug/ml Streptomycin in 0.85% NaCl) and 1.6% agarose for bottom layer and DMEM containing 10% FBS, 2 mM L-glutamine, 0.1 mM non-essential amino acid, 1× pen/strep for upper layer. Compound A solution and upper layer solution containing agarose were mixed, and SW480 cells were added and solidified. Plates were incubated 37° C. at CO₂ incubator for 8 days after solidification at room temperature for 30 min, and colonies were counted under microscope (FIG. 19). The results show that there is synergism of anti-cancer activity between Compound A and 5-FU. LD₅₀ value of Compound A when it was used in combination with 0 μM, 1 μM and 4 μM of 5-FU was 76 μM, 30 μM and 2 μM, respectively.

Example 23 Anti-Angiogenic Activity of Compound E

Tube formation assay was performed using an In Vitro Angiogenesis Assay Kit (Chemicon International, Inc., Temecula, Calif., USA), Briefly, solid gels were prepared according to the manufacturers manual on a 96-well tissue culture plate. HUVEC (1×10⁵ cells/ml) in HuMedia EG-2 medium containing 0-250 μM of vitamin B6 were seeded 100 μl per well onto the surface of the solid gel, ECMatrix™. The cells were incubated with vehicle control, Compound E at 0.1 μM, 0.3 μm, 1.0 μM, 3 μM, and 10 μM, or Fumagilin at 10 μM for 12 h at 37° C. in a CO₂ incubator Tube formation was observed under an inverted light microscope at ×100 magnification. Microscopic fields were photographed with a digital camera. The results show that Compound E inhibited tube formation in a dose-dependent manner (FIG. 20).

Example 24 Efficacy of Compound F in Rat Adjuvant-Induced Arthritis Model

To induce polyarthritis, six-week-old male S.D. rats received intradermal injection (base of tail) of 100 μl of Mycobacterium butyricum (Cat. No. 264010, Difco) in mineral oil (5 mg/ml) on Day 0. The test compound, Compound F, was given once daily at Day 1, 2, 3, 4, 5, 8, 10, 12 and 14 by oral gavage. Non-treated control rats (NT) did not receive Mycobacterium or Compound F. Vehicle control rats (VH) received the pharmacological carrier used for Compound F. For reference, indomethacin (Sigma, 3 mg/kg) was given once daily at Day 1, 2, 3, 4, 5, 8, 10, 12 and 14 by oral gavage. The paw thickness was measured with digital caliper (Mitutoyo, Japan) and the arthritic index was accessed (FIG. 21). Oral treatment of Compound F at the dose of 30 mg/kg and 100 mg/kg significantly ameliorated the increase of paw thickness.

Example 25 The effect of Compound F on Serum TNF-a Concentrations Induced by Intraperitoneal Injection of LPS

Male young ICR mice received intraperitoneal injection of LPS O111:B4), Compound F was administered perorally 60 min prior to LPS challenge and blood was drawn 90 min subsequent to challenge. Vehicle control mice received the pharmacological carrier used for Compound F only. Concentration of TNF-α in the serum was determined by ELISA method. FIG. 22 shows TNF-α level of each group with the error bars representing standard deviations (n=8). For reference, dexamethasone (Dex, Sigma) was treated (15 mg/kg, oral). The results demonstrate that the effect of Compound F reduces LPS-induced TNF-α production in serum in a dose-dependent manner.

Example 26 Inhibition of NF-κb Reporter Activity by Compound F

Stably transfected NF-κB A549 cells were maintained with RPM-1640 containing 10% FBS, 0.1 mM non-essential amino acid, 1× pen/strep and G418 (400 μg/ml). Cells were transferred into each well of 96 well white opaque plates (1×10⁴ cells/well/50 μl) and incubated 24 hr at 37° C. in 5% CO₂ incubator. The test compound, Compound F, was added to each well, and 1 hr later, phorbol 12-myristate 13-acetate (PMA) (10 ng/ml) was added into each well. Plates were incubated further for 6 hr at 37° C. in 5% CO₂ incubator. One hundred microliter of Dual-glo FireFly substrate (Promega) was added and incubated for 10 min. Luminescence of each well was measured with a luminometer (Victor II) (FIG. 23). The results show that Compound F is effective in inhibiting NE-κB transcription which is important in pathogenesis of acute and chronic inflammation.

Example 27 Inhibition of Pro-Inflammatory Cytokine Production by Compound F

LPS-induced TNF-α production in THP-1 cells: THP-1 cells were incubated with 200 nM PMA for 24 hr. Cells were harvested with trypsin and seeded into 96 well tissue culture plates (2×10⁴ cells/well). The test compound, Compound F, was added to each well followed by LPS (100 ng/ml). The cells were further incubated for 6 hr at 37° C. in a CO₂ incubator. Media was collected and concentration of TNF-α was determined with the ELISA kit (OptEIA, BD). IC₅₀ of Compound F was 7.083 μM in this assay (FIG. 24A).

PMA/Ionomycin-induced IL-2 production in Jurkat cells: Jurkat cells were seeded into 96 well tissue culture plates (1×10⁵ cells/well) and treated with the test compound, Compound F, and further incubated for 60 min at 37° C. in a CO₂ incubator. Stimulant (10 ng/ml PMA and 1 μg/ml ionomycin) was added into each well, and the cells were further incubated for 6 hr at 37° C. in a CO₂ incubator. Supernatant was collected and concentration of IL-2 was determined with the ELISA kit (OptEIA, BD). IC₅₀ of Compound F was 8.483 μM in this assay (FIG. 24B).

It will be appreciated that, although specific embodiments of the invention have been described herein for the purposes of illustration, various modifications may be made without departing from the spirit and scope of the invention. Accordingly, the invention is not limited except by the appended claims.

All of the above U.S. patents, U.S. patent application publications, U.S. patent applications, foreign patents, foreign patent applications and non-patent publications referred to in this specification and/or listed in the Application Data Sheet are incorporated herein by reference.

From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims. 

1. A compound having the following formula (I):

wherein R_(a) is indolyl substituted with one or more substituents selected from the group consisting of alkyl, acyl, oxo, aryl, arylalkyl, acyloxyalkyl, amidino, alkoxy, cyano, guanidino, alkylguanidino, dialkylguanidino, halo, hydrazinyl, hydroxyl, pyridinyl, nitro, —OC(O)—R^(d), —N(R^(d))₂, —C(O)OR^(d), —C(O)N(R^(d))₂, —N(R^(d))C(O)OR^(d), —N(R^(d))C(O)R^(d), —N(R^(d))S(O)_(t)R^(d) (where t is 1 or 2), —S(O)_(t)OR^(d) (where t is 1 or 2), —S(O)_(p)R^(d) (where p is 0, 1 or 2), and —S(O)_(t)N(R^(d))₂ (where t is 1 or 2) where each R^(d) is independently hydrogen, alkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl; R_(b) is hydrogen; R_(c) is hydroxyl, amidosulfonate, phosphate, monosodiumphosphate, or disodiumphosphate, as an isolated stereoisomer or a mixture of stereoisomers or as a pharmaceutically acceptable salt.
 2. The compound of claim 1 wherein R_(a) is substituted indolyl substituted with one or more substituents selected from the group consisting of alkyl, acyl, aryl, arylalkyl, alkoxy, cyano, halo, pyridinyl, —S(O)₂R^(d) where R^(d) is alkyl or aryl.
 3. A compound selected from the group consisting of:


4. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier.
 5. A compound having the following formula (II):

wherein R_(a) is indolyl substituted with one or more substituents selected from the group consisting of alkyl, acyl, oxo, aryl, arylalkyl, acyloxyalkyl, amidino, alkoxy, cyano, guanidino, alkylguanidino, dialkylguanidino, halo, hydrazinyl, hydroxyl, pyridinyl, nitro, —OC(O)—R^(d), —N(R^(d))₂, —C(O)OR^(d), —C(O)N(R^(d))₂, —N(R^(d))C(O)OR^(d), —N(R^(d))C(O)R^(d), —N(R^(d))S(O)_(t)R^(d) (where t is 1 or 2), —S(O)_(t)OR^(d) (where t is 1 or 2), —S(O)_(p)R^(d) (where p is 0, 1 or 2), and —S(O)_(t)N(R^(d))₂ (where t is 1 or 2) where each R^(d) is independently hydrogen, alkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl; R_(c) is hydroxyl, amidosulfonate, carbonylsulfamate, phosphate, monosodiumphosphate, or disodiumphosphate, as an isolated stereoisomer or a mixture of stereoisomers or as a pharmaceutically acceptable salt.
 6. The compound of claim 5 wherein R_(a) is substituted indolyl substituted with one or more substituents selected from the group consisting of alkyl, acyl, aryl, arylalkyl, alkoxy, cyano, halo, pyridinyl, —S(O)₂R^(d) where R^(d) is alkyl or aryl.
 7. A compound selected from the group consisting of:


8. A pharmaceutical composition comprising a compound according to claim 5 and a pharmaceutically acceptable carrier. 